Summary & Overview
HCPCS G9017: Amantadine Hydrochloride Oral 100 mg
HCPCS Level II code G9017 denotes a 100 mg oral unit of amantadine hydrochloride supplied specifically for use in a Medicare-approved demonstration project. As a demonstration-specific HCPCS Level II code, G9017 is important for tracking medication participation in federally sanctioned research initiatives and for ensuring appropriate billing and reporting within those programs. Nationally, such demonstration project codes affect program accounting, supply chain reporting, and program evaluation rather than routine clinical reimbursement.
Key payers commonly considered in discussions of HCPCS demonstration codes include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find context on the clinical purpose of the code, the typical outpatient/ambulatory sites where the medication would be dispensed, and the implications for billing systems when handling demonstration-project pharmaceuticals. The publication outlines benchmarking considerations, how demonstration-specific HCPCS codes are used distinct from standard outpatient drug codes, and the policy context that governs Medicare-approved demonstration projects.
This summary is intended for administrators, coders, and policy stakeholders seeking concise guidance on the role and national significance of HCPCS Level II code G9017 in demonstration project workflows.
Billing Code Overview
HCPCS Level II code G9017 represents Amantadine hydrochloride, oral, per 100 mg provided for use in a Medicare-approved demonstration project. The service type is oral medication dispensing and administration for a demonstration research program. The typical site of service is outpatient or ambulatory settings where oral pharmaceuticals are dispensed or administered for demonstration projects, including clinic pharmacies and outpatient infusion/medication units.
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Clinical & Coding Specifications
Clinical Context
A Medicare beneficiary enrolled in a CMS-approved demonstration project is being treated with oral amantadine hydrochloride for management of Parkinson disease motor symptoms or drug-induced extrapyramidal symptoms. Typical patient is an older adult with established neurologic diagnosis such as Parkinson disease who attends a neurology clinic visit for medication management. The workflow: clinician documents indication, past response to dopaminergic therapy, and rationale for use of amantadine; prescriber writes an order for oral amantadine hydrochloride, documented as G9017 units per 100 mg; pharmacy dispenses medication per the demonstration project protocol; clinician documents follow-up plan and monitors for side effects (confusion, hallucinations, peripheral edema, orthostatic hypotension) and renal function for dose adjustment. Visits may include baseline and periodic medication reconciliation, medication counseling, and assessment of motor function using standard clinical scales.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
24 | Unrelated Evaluation and Management service by the same physician during a postoperative period | Use if an unrelated E/M is provided during a postoperative global period when G9017 is billed separately as part of medication management outside postoperative care |