CHAPTER 518 — Pharmacy Services (Outpatient Pharmacy Coverage, Prior Authorization, IHPT, and Related Requirements)
Customize your policy alerts
Sign up for all West Virginia Bureau for Medical Services (Department of Human Services) policy alerts
Know when West Virginia Bureau for Medical Services (Department of Human Services) releases new policies or updates existing guidance.
Monitor payer policy activity
Defines West Virginia Medicaid coverage, limits, prior authorization, and provider/member requirements for outpatient pharmacy services including OTCs, diabetic supplies, home infusion, and in-home parenteral therapy. Applies to providers and Medicaid members served by the West Virginia Bureau for Medical Services.
No material clinical or coverage changes in this revision.
Coverage Criteria and Program Rules
General outpatient pharmacy coverage
Covered when ALL of the following are met (general outpatient pharmacy program):
Based on CHAPTER 518.1 covered services
IHPT coverage criteria
IHPT is covered when ALL of the following are met:
CHAPTER 518.1.5 and PRIOR AUTHORIZATION
See prior authorization and IHPT billing guidance
IHPT Eligibility
Members receiving IHPT must meet ALL of the following:
CHAPTER 518 MEMBER REQUIREMENTS
CHAPTER 518 MEMBER REQUIREMENTS
CHAPTER 518 MEMBER REQUIREMENTS
CHAPTER 518 MEMBER REQUIREMENTS
Prospective DUR
Prospective DUR at pharmacy POS is applied to identify potential therapy problems; dispensing pharmacist must evaluate and decide whether to fill based on professional judgment.
The pharmacist uses POS information and professional judgment to determine appropriateness and intervenes with prescriber and/or member if a problem is suspected.
Retrospective DUR
Retrospective DUR identifies patterns of fraud, abuse, overuse, or inappropriate care and generates provider/pharmacist letters.
Monthly committee review as described in CHAPTER 518.5.2
Pharmacy Lock-in Program
Pharmacy lock-in is applied when criteria for inappropriate controlled substance utilization are met.
If criteria are met, member may be assigned to a single pharmacy; pharmacy participation is voluntary and member may be asked to select a pharmacy.
Pharmacy Certification & Enrollment
Pharmacy certification and enrollment requirements for reimbursement.
Failure to have current license/permit on file results in non‑reimbursement until documentation received.
340B Program Billing
340B participating pharmacies billing requirements.
Using both '20' and '08' together will result in claim denial; providers must ensure HRSA listing of participation is current.
Returns and Record Retention
Prescription returns and recordkeeping.
Maintain log for five years to support reversals or disputes.
Member Counseling
OBRA '90 requires pharmacists to offer counseling to Medicaid members; counseling must include:
BMS may audit compliance; West Virginia BOP monitors counseling activities.
Tamper-Resistant Prescription Requirement
Tamper‑resistant written prescription requirements under OBRA '90 — all written prescriptions for WV Medicaid must meet ALL three CMS characteristics:
Computer‑generated/ePrescribed prescriptions may comply if they include equivalent industry‑recognized features.
Member-specific coverage
Coverage rules by member category and program:
CHAPTER 518.15.1
CHAPTER 518.15.2
CHAPTER 518.15.3
Limited Pharmacy Services
Limited Pharmacy Services (Ryan White) eligibility and coverage:
CHAPTER 518.16.1
Claims for vaccines have separate submission instructions.
Non-Medicaid state-funded programs
Special state‑funded coverage programs and requirements:
Claims subject to Medicaid rules; state letter must accompany claims when required.
CHAPTER 518.16.3 and 518.16.4 context
Billing and Dispensing Criteria
Coverage, billing and dispensing rules and limits:
Pharmacist must notify prescriber and adjust dispensing to Medicaid limits if needed; see CHAPTER 518.18.9
Compounding is integral and must not be billed separately; see CHAPTER 518.18.10
Violations are subject to audit, recovery, or provider suspension/termination (CHAPTER 518.18.11 and 518.18.11 automated refill prohibition).
See CHAPTER 518.18.12 and 518.18.13 for documentation and exclusions.
Lost/Stolen Medication Replacement
Replacement of lost or stolen medications is permitted when the following ALL apply
In natural disasters BMS handles exceptions case‑by‑case (CHAPTER 518.18.12)
Wasted Medication
Wasted medication replacement is considered on a case-by-case basis but with explicit exclusions
CHAPTER 518.18.13
Ingredient Cost Reimbursement Options
Reimbursement for covered outpatient drugs is the lower of the following options (in the order presented):
FUL/SMAC exceptions permit handwritten physician 'brand medically necessary' certification to override; NADAC files updated weekly (CHAPTER 518.19.1 and CHAPTER 518.19.1 exceptions).
Dispensing Fee Rules
Dispensing fee rules and application:
Compounding fee is additive ($6.00) and compounding is integral to the prescription service (CHAPTER 518.19.2).
Co-payment Requirements and Exemptions
Co-payment requirements and exemptions:
See CHAPTER 518.19.3 and 518.19.3 exemptions for full list.
Third-Party Liability / Coordination of Benefits
Third‑party liability and coordination of benefits rules:
No Medicaid reimbursement if service is responsibility of workers' compensation; see CHAPTER 518.19.4.
Medicare Coordination
Medicare coordination rules for Part B and Part D:
See CHAPTER 518.19.5 for Part B processes.
See CHAPTER 518.19.6 for Part D rules.
In-Home Parenteral Therapy (IHPT) Billing
Billing rules specific to In‑Home Parenteral Therapy (IHPT):
Do not bill diluent separately if compounding fee requested; units defined per First Data Bank conventions.
Total parenteral nutrition (TPN) supplies are classified as durable medical equipment (DME) and are not covered as pharmacy point‑of‑sale (POS) services. Providers should bill TPN supplies through the appropriate DME processes rather than the pharmacy POS.
Diabetic testing supplies and syringes/needles are covered through the outpatient pharmacy program for eligible members, but are not covered pharmacy services for members residing in skilled nursing facilities or ICF/IID facilities. For community members, quantity limits apply (e.g., 150 blood/urine strips and 200 lancets per 30 days for insulin‑dependent members); quantities above these limits require prior authorization.
The policy lists multiple exclusions. Notable non‑covered items include drugs from manufacturers not enrolled in the CMS drug rebate program; agents for weight loss, cosmetic/hair growth, fertility, or erectile dysfunction; drugs identified as less‑than‑effective (DESI); investigational products or investigational uses; off‑label uses not supported by official compendia or peer‑reviewed literature; expired drugs; shipping/delivery charges; herbal/homeopathic products; nutritional supplements and free samples; and certain vaccine and methadone exclusions. Additionally, drugs that cause therapeutic or ingredient duplication or otherwise trigger DUR rules and drugs that are not medically necessary are excluded.
The Bureau for Medical Services does not enroll dispensing physicians as a pharmacy provider type. As a result, reimbursement for self‑administered outpatient prescription drugs is limited to licensed and participating pharmacies; claims submitted by dispensing physicians who are not enrolled as pharmacies will not be reimbursed.
For dual‑eligible members Medicare is the primary payer for prescription drugs (Part D or Part C). Medicaid will not reimburse Medicare Part D or Part C co‑payments and will not act as secondary payer on drugs covered by Medicare Part D or Part C. Medicaid only covers drugs in Medicare‑excluded categories where applicable.
Members who are incarcerated are excluded from pharmacy benefits until release. Claims with dates of service during a period of incarceration will be denied. If the member has been released prior to an eligibility update, positive identification is required and an override may be requested from the pharmacy prior authorization vendor help desk.
Drugs repackaged by repackagers are generally not covered if the repackager has not signed a CMS drug rebate agreement; repackager NDCs cannot be used to bill Medicaid. All pharmacy claims must report the 11‑digit NDC printed on the stock container in which the drug was purchased. In addition, supplies or items identified as part of a compounded prescription (e.g., suppository molds) are not reimbursable.
Requests to replace wasted medications are considered on a case‑by‑case basis. Members may receive replacement when medication was wasted due to improper use or storage, subject to review and counseling. Replacement requests caused by improper storage or delivery by the pharmacy or improper handling by the administrating provider will be denied. For lost or stolen controlled substances, replacement requires a police report and prescriber agreement and is limited to one occurrence per drug per year.
Effective July 1, 2024, BMS will deny prescriptions submitted by medical residents who do not have a valid educational permit on file with the BMS fiscal/provider enrollment agent. Prescriptions from residents must be submitted only when the resident's educational permit is recorded in the provider enrollment system to be eligible for reimbursement.
Drug Utilization Review (DUR) edits are used to identify clinically inappropriate therapy. Drugs that trigger DUR events — including therapeutic duplication, ingredient duplication, early refills, or other DUR flags — are considered not medically necessary and are not covered unless appropriately resolved (for example, via an approved override or prior authorization when supported by documentation).
Automatic refill programs and fills performed without an explicit refill request from the member or the member's responsible party are prohibited. Medicaid will not pay for prescriptions filled without an explicit request; such fills are subject to recovery. Pharmacies must obtain an explicit request for each refill, and any automated refill or automatic shipment practice may lead to audit, claim recovery, or provider action.
Coding, Billing Values, and Code Requirements
| 420-DK | Claim Segment-Submission Clarification Code — Use value 20 in Position 1 or 2 |
| 423-DN | Pricing Segment- Basis of Cost Determination — Use value 08 |
| J-codes | Drugs billed with J Codes/HCPCS are covered by managed care and cannot be billed to FFS at point of sale |
| NCPDP Version D.0 | Accepted POS transaction standard for online pharmacy claims |
| Batch Version 1.1 | Accepted NCPDP batch submission standard |
| 11-digit NDC | NDC printed on the stock container in which the drug was purchased — required on all pharmacy claims |
| NDC | Active ingredient(s) billed using the NDC and respective unit of use for IHPT |
| NCPDP Version D.0 | Electronic billing standard for IHPT claims |
| NCPDP 1.1 batch | Approved paper claim/batch system for IHPT |
| NCPDP compound indicator | Indicator to be used when product includes multiple agents (per guidance) |
Prior Authorization, Documentation, and Provider Responsibilities
Prior authorization required for infusion and IHPT
Drugs used for home infusion therapy and all In-Home Parenteral Therapy (IHPT) services require prior authorization and must be requested through the BMS-designated pharmacy prior authorization vendor; the request must justify the need and, for infusion drugs, explain why oral therapy is unsuitable.
- Requests must be made through the pharmacy prior authorization vendor using approved Prior Authorization Forms available on the BMS website.
Prior authorization for diabetic supply overages
Prescriptions for diabetic testing supplies or syringes/needles that exceed the stated quantity limits (e.g., 150 test strips/30 days, 200 lancets/30 days for insulin-dependent members) require prior authorization through the pharmacy prior authorization vendor.
- Limits for insulin-dependent members: urine/blood test strips 150/30 days; lancets 200/30 days; insulin syringes 100/30 days; pen needles 100/30 days.
- Requests for quantities greater than these limits must be submitted to the pharmacy prior authorization vendor.
Prior authorization required for IHPT and certain drugs
All IHPT services and certain drugs require prior authorization via the pharmacy prior authorization vendor; prior authorization may be initiated by the dispensing pharmacist, prescriber, or the prescriber's designee and, when complete, will be addressed within 24 hours.
- Signed physician orders for compounded IHPT medications must be provided if compounding reimbursement is requested.
- If complete information is provided, requests will be addressed within 24 hours; emergent 72-hour supplies permitted while PA is pending.
Prospective DUR edit override and cash-payment risk
When a prospective DUR message requires an override, the dispensing pharmacist may need to contact the pharmacy prior authorization vendor Help Desk to obtain an edit override; requests to override edits after service has been rendered will be denied except for retroactive eligibility, and members paying cash to bypass PA/limits may cause Medicaid to deny coverage.
- Pharmacists should use DUR outcome and intervention codes when processing prospective DUR messages and call the prior authorization vendor Help Desk when instructed.
- Medicaid may deny coverage of controlled substances when members pay cash to circumvent prior authorization or quantity limits.
Prior authorization required
Certain drugs and additional supplements (for example, ESRD-related vitamins/minerals) require prior authorization through the Rational Drug Therapy Program (RDTP) or other designated prior authorization pathways; providers must contact the appropriate prior authorization vendor to confirm eligibility or diagnosis.
- For ESRD supplements the prescriber must contact the RDTP by fax, phone, or mail to confirm the ESRD diagnosis.
- Limited Pharmacy Services brand-name drugs with generic equivalents require prior authorization.
Prior authorization subject to standard Medicaid rules
All pharmacy claims are subject to standard Medicaid rules including DUR edits and prior authorization requirements; providers must follow POS electronic submission or approved paper claim procedures and secure any required prior authorizations before rendering services.
- Claims must be filed within 12 months from the date of service and must accurately report NDC, units, days' supply and other required data.
- If the service is provided before PA is obtained, the member should be informed they may be financially responsible.
IHPT Prior Authorization
IHPT drug components and compounding fees require prior authorization through the pharmacy prior authorization vendor; billing and units submitted for payment must match the authorized amount and duration (maximum 34 days) and the vendor issues compounding-fee authorization upon receipt of the signed physician order.
- Units billed must reflect actual vials or milliliters used and must match the prior authorization.
- Do not bill diluent separately if reimbursement for a compounding fee is requested; compounding fee includes supplies and professional services.
Prior authorization vendor
BMS designates a Pharmacy Prior Authorization Vendor to perform prior authorizations for prescription drugs; providers must use that vendor and its approved forms/processes when requesting prior authorization.
- Prior authorization requests may be made by telephone, fax, or mail; Prior Authorization Forms are available on the BMS website.
- It is the responsibility of the prescribing provider or pharmacist to obtain authorization before rendering the service.
PDL non-preferred drug access
Non-preferred drugs on the Preferred Drug List (PDL) remain accessible through the prior authorization process; providers should submit PA requests when non-preferred agents are clinically indicated.
- The PDL and criteria for coverage of non-preferred drugs are available on the BMS website.
Preferred drug list step
When appropriate, providers must try PDL-preferred drugs before non-preferred drugs will be approved; this step requirement is enforced via the prior authorization criteria developed by the DUR/P&T process.
- PDL-preferred drugs are selected by the P&T Committee and the list is updated at least annually.
DUR Board role in PA criteria
The DUR Board assists BMS in defining criteria for drugs that require prior authorization and may thus enable step or coverage rules; providers should refer to BMS criteria informed by the DUR Board when requesting authorization.
- DUR Board meeting agendas and criteria information are available on the BMS website.
Generic-first requirement and brand justification
Formulary drugs must be dispensed in generic form when a generic equivalent is available; dispensing a brand-name product when a generic exists requires justification per the general pharmacy instructions and prior authorization where applicable.
- Brand name use must be justified as referenced in the general pharmacy instructions; brand justification procedures apply when submitting claims.
IHPT prior authorization documentation
Prior authorization requests for IHPT must be submitted through the pharmacy prior authorization vendor using the approved forms posted on the BMS website; signed physician orders for compounded IHPT medications are required when compounding reimbursement is requested.
- Prior Authorization Forms (Form IV-1) must be submitted via fax or mail when required by the vendor.
- The prior approval is effective from the date of the physician's original order and changes in therapy require new prior authorizations.
Required contents for prior authorization requests
Prior authorization requests must include member name/address/Medicaid ID, drug name/strength/dosage/duration, diagnosis, pertinent laboratory information, justification for drug use, return fax number, and the signature of the prescriber or pharmacist.
- Incomplete PA requests may delay the 24-hour turnaround; the provider is responsible for obtaining the authorization before rendering the service.
Annual permit filing requirement
Pharmacies must file a copy of their current West Virginia State Board of Pharmacy permit with BMS annually; failure to have a current license/permit on file will result in non-reimbursement until BMS receives documentation.
- Out-of-state pharmacies shipping into West Virginia must be licensed in their state and hold a WV BOP permit as applicable.
340B claim submission values and denial risk
340B-participating pharmacies must bill each POS claim using either Claim Segment-Submission Clarification Code value '20' (420-DK) OR Pricing Segment- Basis of Cost Determination value '08' (423-DN) to identify 340B claims and must submit actual acquisition costs; using both values together will result in claim denial.
- Submission of invoices may be required for audit and invoices/actual acquisition cost must be available on request.
- Per NCPDP guidance the '20' and '08' values are mutually exclusive; using both leads to denial.
A log of prescriptions returned to stock
A returns-to-stock log of prescriptions filled but not dispensed must be maintained and retained by the pharmacy for five years to support timely reversals and audits; claims must be reversed within 15 days when not dispensed.
- Maintain the returns log for five years for auditing purposes and reverse claims within 15 days of the fill when not dispensed.
Retention of delivery and returns logs (5 years)
Pharmacies must retain delivery signature logs (proof of delivery) and returned-to-stock logs for five years to support reversals or disputes; absence of member signature as definitive proof of delivery may lead to reimbursement being withheld or claim reversal.
- In disputes the only definitive proof of delivery accepted is a copy of the member's signature on the delivery log.
- Recommendation: retain signature logs for five years to support any delivery disputes.
Certain state-funded eligibility requires eligibility letter and paper claim
For state-funded non‑Medicaid programs, providers must have the written eligibility communication/authorization letter and may be required to submit claims on the approved paper claim form with the eligibility letter attached as instructed.
- Examples include letters with prefix codes (e.g., '39', '15', '38') that identify covered services and billing instructions.
- Claims for these programs must follow Medicaid coverage rules and may require paper submission with the authorization letter attached.
Presentation of eligibility for certain state-funded programs
When members present for services under certain state-funded programs (emergency assistance, juvenile services, adult family/protective services), the member must present the eligibility letter at point of service and providers must follow the submission instructions (POS or approved paper form) noted on the letter.
- Letters include identification prefixes (e.g., '17' for juvenile services) and specify whether claims should be submitted online or on paper with the letter attached.
Lost/Stolen Medication Documentation
Pharmacies must retain a copy of the police report when replacing stolen controlled substances; the prescribing practitioner must agree to replace the lost/stolen medication and replacements are limited to one occurrence per drug per year.
- Pharmacy must retain the police report copy for audit purposes.
- Approvals for lost/stolen controlled substances are limited to one occurrence per drug per year.
IHPT compounding fee documentation and unit matching
IHPT compounding fee reimbursement requires submission of a copy of the signed physician order to the pharmacy prior authorization vendor; units billed must match the prior authorization and represent actual vials or milliliters used.
- The compounding fee includes supplies and professional services; do not bill the diluting agent separately if compounding fee reimbursement is requested.
- Units are defined per First Data Bank product classification and must match the amount authorized by the prior authorization vendor.
State Plan references for documentation and billing
Providers should follow the State Plan sections referenced in the chapter for documentation and billing rules governing pharmacy services and pharmacist vaccine administration.
- State Plan sections referenced include reimbursement and vaccine-administration rules; follow those sections when preparing documentation and claims.
Excluded or unenrolled prescribers cause denial
Prescriptions issued by prescribers excluded from federal health programs or by prescribers not enrolled with West Virginia Medicaid will be denied reimbursement; ensure prescribers are enrolled and not excluded before dispensing.
- Verify prescriber enrollment and exclusion status prior to filling to avoid claim denial.
Third‑party vendor PAs and after-the-fact requests will be denied
Prior authorization requests submitted by third‑party vendors or contractors will be denied; prior authorization requests made after the service is rendered will be denied (except for case-by-case consideration with backdated eligibility).
- It is the provider's responsibility (physician or pharmacist) to obtain authorization before rendering the service.
- Backdated/retroactive eligibility cases may be considered on a case-by-case basis.
Edit override requests after service are denied (except retroactive eligibility)
Requests for edit overrides after the service has been rendered are generally denied except in cases of retroactive eligibility; pharmacists should obtain any required override prior to dispensing.
- Use DUR outcome/intervention codes and contact the prior authorization vendor Help Desk when instructed to obtain an override before dispensing.
Do not use both NCPDP values '20' and '08' together
Using both NCPDP 340B identification values '20' (Claim Segment-Submission Clarification Code) and '08' (Pricing Segment- Basis of Cost Determination) together on the same claim is prohibited and will result in denial of the claim.
- Use either '20' OR '08' per NCPDP guidance to identify 340B claims; if a claim is later identified as 340B it must be reversed and rebilled using value '08' only.
Denial risk when member pays cash to bypass PA/limits
Medicaid may deny coverage of controlled substances when the member is found to be paying cash to bypass prior authorization and/or quantity limit requirements; pharmacies are encouraged to report suspected cash-pay circumvention to BMS.
- Report suspected cash payments intended to bypass Medicaid using the Cash Waiver Form available on the BMS website.
Delivery proof (member signature) required to avoid reversals
Pharmacies must maintain proof of delivery (member signature) for shipped medications; in disputes lack of a delivery signature may result in reversal of reimbursement and reimbursement will be withheld when signature proof is not provided.
- Maintain a delivery signature log for five years to support disputes and potential reversals.
- Claims for medications not received by the member may be reversed to allow a local pharmacy to meet member needs.
Claims during incarceration will be denied
Medicaid claims with dates of service during a period of incarceration will be denied; if the member has been released before the restriction is updated, obtain positive identification and contact the prior authorization vendor Help Desk for overrides as instructed.
- Pharmacists must verify incarceration status before dispensing and follow override procedures if applicable.
Denial risks: eligibility, prescriber NPI, and permit issues
Claims may be denied for eligibility problems, incorrect prescriber identification (non-prescribing NPI entities), or provider enrollment/permit issues; ensure valid member eligibility, prescribing NPI, and current pharmacy permit are on file prior to billing.
- Only prescribing NPI entities are permissible on POS claims; claims with non-prescribing NPI entities will be denied.
- Pharmacy payments may be withheld if the current license/permit is not on file with BMS.
Denial for replacements caused by pharmacy/provider error
Requests to replace wasted medications caused by improper storage or delivery by the pharmacy or improper handling by the administrating provider will be denied; replacements due to member improper use/storage may be considered case-by-case.
- Inform members on proper storage and device use; replacements caused by pharmacy/provider error are not payable.
Denial risk for medical residents without educational permit
Effective July 1, 2024, prescriptions submitted by medical residents without a valid educational permit on record with BMS's fiscal/provider enrollment agent will be denied; verify resident permits prior to dispensing.
- Claims submitted by medical residents without a valid educational permit on file will be denied beginning July 1, 2024.
Step Therapy and Formulary Requirements
| Requirement | Summary |
|---|---|
| Step therapy requirement (PDL-preferred first) | When appropriate, Preferred Drug List (PDL)–preferred drugs must be tried prior to approval of non‑preferred drugs; non‑preferred agents remain available via prior authorization. |
| Requirement | Policy detail |
|---|---|
| Generic‑first dispensing | Formulary drugs must be dispensed in generic form when a generic is available; dispensing the brand product when an interchangeable generic exists requires prior authorization. |
| Brand with generic equivalent | Brand‑name drugs that have generic equivalents require prior authorization for dispensing to Limited Pharmacy Services participants (applies generally where generics available). |
Quantity Limits and Emergency Supplies
Site-of-Care Requirements for IHPT
IHPT member must reside in private home or domiciliary care
Members receiving IHPT must reside in a private home or domiciliary care facility; institutional settings such as hospitals, SNFs, ICF/IID group homes, rehabilitation centers, and other institutional settings are not eligible for IHPT.
IHPT covered only in private home/domiciliary settings
IHPT is covered only when the member resides in a private home or domiciliary care setting; institutional settings are excluded from IHPT coverage.
IHPT billing/delivery for home use — PA up to 34 days
IHPT drugs and compounding may be billed and delivered for use at the member’s home under prior authorization for a maximum duration of 34 days per prior authorization.
- Billing shall correspond to therapy for a duration of up to 34 days as prior authorized.
Defined Terms
Documentation, Retention, and Proof Requirements
Returned-to-stock log retention — 5 years
Maintain prescription returned-to-stock logs for five years to support audits and timely reversals.
Delivery signature log retention — 5 years
Maintain delivery signature logs for five years to support reversals or disputes; the member signature is the definitive proof of delivery in disputes.
Retain police report for stolen controlled substances
Retain a copy of the police report for stolen controlled substances for audit purposes and ensure the prescribing practitioner agrees to replacement prior to dispensing a replacement.
Signed physician order required for IHPT compounding fee PA
IHPT compounding fee authorization requires submission of a copy of the signed prescribing physician's order to the Pharmacy Prior Authorization Vendor; units billed must exactly match the prior authorization.
Billing, Reimbursement Methods, and Fees
Ingredient cost pricing hierarchy and reimbursement calculation order (NADAC/WAC/FUL/SMAC)
Ingredient cost pricing hierarchy and reimbursement calculation order (used when computing ingredient reimbursement):
FUL and SMAC have physician 'brand medically necessary' handwritten exception; NADAC files updated weekly (CHAPTER 518.19.1 and CHAPTER 518.19.1 exceptions).
Dispensing fee rules — professional dispensing fee and additional compounded fee
Dispensing fee application and additional fees:
Compounding fee is included in dispensing fee and compounding is integral — not billed separately (CHAPTER 518.19.2).
Claims denied during incarceration periods
Claims with dates of service during incarceration will be denied; ensure member eligibility status before billing.
Edit override requests after service are generally denied
Requests to override edits after the service has been rendered are generally denied except for retroactive eligibility; obtain necessary overrides prior to dispensing when possible.
Policy Revision History
Entire Chapter titled 'Pharmacy Services' became effective; initial chapter publication and multiple section changes recorded (including brand vs generic, 340B program, ingredient cost, dispensing fee).
Chapter effective date entry recorded for December 1, 2020 as part of the change log history.
Updates to section 518.15.3 concerning Medicaid members with End Stage Renal Disease were recorded in the chapter change history.
Updates to section 518.16.1 Limited Pharmacy Services (Ryan White Program) claims were recorded in the chapter change history.
Multiple updates effective January 1, 2022 including tobacco cessation specifics, HPV vaccine language additions, diabetic supply list hyperlink, out-of-state pharmacy enrollment policy, 340B billing requirements, member counseling clarification, and co-payment postpartum updates.
Additional updates to tobacco cessation, buprenorphine coverage, certification, 340B billing, member counseling, and co-payment policy noted in the change history effective March 16, 2023.
Effective July 1, 2024, BMS will deny prescriptions submitted by medical residents without a valid educational permit on record with its fiscal/provider enrollment agent.
Entire Chapter 'Pharmacy Services' updated and republished with an effective date of July 1, 2026; includes co-payment exemptions updates effective July 1, 2026.
OpenPayer is powered by Trek Health's payer performance platform. Trek continuously ingests, validates, and normalizes Transparency in Coverage data alongside payer policies and other commercial payer data to create a structured payer intelligence foundation. OpenPayer uses this foundation to deliver personalized search results, dynamically generated policy pages, and tailored policy monitoring based on each user's payers, specialties, billing codes, and areas of interest. The same intelligence powers broader payer performance workflows, including reimbursement benchmarking, contract evaluation, payer negotiations, and financial decision-making.