Summary & Overview
HCPCS C9065: Injection, Romidepsin (Liquid), 1mg
HCPCS Level II code C9065 designates the supply of romidepsin in a non-lyophilized (liquid) formulation, billed per 1 mg. Romidepsin is an antineoplastic agent used in oncology care, and precise billing for drug formulation and unit dosing is essential for claims processing, clinical recordkeeping, and national cost benchmarking. This code matters nationally because injectable oncology therapies represent a significant and growing component of specialty drug spend and utilization in outpatient infusion settings.
Key payers included in this analysis are Aetna, Blue Cross Blue Shield, Cigna, UnitedHealthcare, and Medicare. Readers will find a focused overview of clinical context for romidepsin billing, expected sites of service, and the typical service type. The publication summarizes national implications for reimbursement administration, highlights common billing modifiers and claim considerations where available, and points to areas where policy updates or payer-specific coverage rules may affect payment and utilization. Where input data is missing, the content notes that information is not available. The reader will gain a concise resource for understanding HCPCS Level II code C9065 and its role in outpatient chemotherapy billing and claims workflow.
Billing Code Overview
HCPCS Level II code C9065 represents injection, romidepsin, non-lyophilized (e.g. liquid), 1mg. This billing code denotes a chemotherapy/antineoplastic injectable medication formulation measured per milligram and is used to report administration of romidepsin in its liquid (non-lyophilized) form.
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Service type: Medication administration / drug supply for chemotherapy
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Typical site of service: Infusion center, hospital outpatient department, or other outpatient clinical settings where intravenous chemotherapy is administered
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Clinical & Coding Specifications
Clinical Context
A typical patient is an adult with a confirmed peripheral T-cell lymphoma or cutaneous T-cell lymphoma who is scheduled to receive intravenous romidepsin as part of systemic chemotherapy. The patient arrives to an outpatient infusion center or hospital outpatient department accompanied by nursing staff and an oncology advanced practice provider. Pre-infusion evaluation includes vital signs, review of baseline labs (complete blood count, comprehensive metabolic panel, liver function tests, electrolytes, and magnesium), ECG review for QTc prolongation risk, and verification of current medications for potential interactions. The romidepsin product described by C9065 is supplied as a non-lyophilized (liquid) formulation dosed per milligram; the order is calculated based on the patient’s body surface area and prescribed mg per dose schedule (for example, 14 mg/m2 on specified days of a 28-day cycle).
During the visit, an IV or implanted port is accessed, and the medication is prepared by pharmacy under sterile conditions. Nursing documents time of infusion start/stop, lot number, and exact milligrams administered to support billing of C9065 per 1 mg units. The infusion is typically administered in an outpatient infusion center, ambulatory infusion suite, or hospital-based infusion clinic. Post-infusion monitoring includes assessment for infusion reactions, laboratory trends, and counseling on adverse effects such as nausea, fatigue, cytopenias, and electrocardiographic changes. Documentation required in the medical record to support billing includes the medication name and formulation, total milligrams administered, date and time of service, infusion site, lot/serial numbers, and clinical rationale tied to an appropriate ICD-10 diagnosis for an FDA‑approved or off-label indication as directed by the treating oncologist.
Coding Specifications
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