Summary & Overview
HCPCS G9019: Oseltamivir phosphate, oral, 75 mg
HCPCS Level II code G9019 designates a 75 mg unit of oral oseltamivir phosphate provided under a Medicare-approved demonstration project. The code captures the dispensing of an antiviral agent used for treatment or prophylaxis of influenza within a structured demonstration setting and is relevant where program-specific billing rules apply. Nationally, use of demonstration-specific HCPCS codes like G9019 matters for tracking program participation, ensuring appropriate reimbursement under demonstration rules, and monitoring access to antiviral therapy during targeted initiatives.
Key payers discussed include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise overview of clinical context and service setting, plus what to expect in associated billing — including where to look for benchmarks and policy updates and how demonstration designations affect claim reporting. The publication outlines the code’s clinical purpose, common sites of service, and the types of information typically required for claims involving demonstration project medications. If specific payer policies, modifiers, taxonomies, or related diagnosis coding are not provided here, the section notes that those details are not available in the input.
Billing Code Overview
HCPCS Level II code G9019 represents oseltamivir phosphate, oral, per 75 mg, designated for use in a Medicare-approved demonstration project. The medication is an oral antiviral agent commonly used to treat and prevent influenza; this HCPCS code documents the dispense of a 75 mg unit within the context of the demonstration.
Service Type: Pharmaceutical dispensing / outpatient oral antiviral therapy
Typical Site of Service: Outpatient clinic, pharmacy, or other outpatient dispensing site
Data not available in the input.
Clinical & Coding Specifications
Clinical Context
A 68-year-old Medicare beneficiary presents to a primary care clinic during influenza season with 48 hours of acute onset fever, cough, myalgias, and malaise. The clinician performs a rapid influenza diagnostic test or clinical assessment consistent with uncomplicated influenza A or B and determines antiviral therapy is appropriate under a Medicare-approved demonstration project. The patient receives a single oral dose of antiviral medication dispensed on-site or provided as a take-home supply. Clinical workflow includes evaluation and documentation of symptom onset and eligibility for antiviral treatment, informed consent when required by the demonstration project, medication administration or dispensing, medication counseling regarding dosing and side effects, and documentation of the demonstration project identifier and billing code on the claim.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
25 | Significant, separately identifiable evaluation and management (E/M) service by the same physician on the day of a procedure | Use when a separate E/M visit is performed and documented in addition to administration or dispensing of antiviral therapy. |
59 | Distinct procedural service |