Summary & Overview
HCPCS Level II C9176: Tc-99m from Domestic Non-HEU Mo-99, Cost Recovery Add-On
HCPCS Level II code C9176 identifies a full cost recovery add‑on for a per‑study dose of technetium‑99m derived from domestically produced non‑HEU molybdenum‑99 (minimum 50%). This code matters nationally as supply chain shifts toward non‑HEU Mo‑99 production and efforts to ensure sustainable domestic radiopharmaceutical supplies affect pricing, hospital budgeting, and access to nuclear medicine services. The add‑on nature of the code targets the radiopharmaceutical component of nuclear imaging and therapy rather than technical or professional service components.
Key payers referenced in this analysis include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find benchmarks for how this add‑on is handled in payer reimbursement policies, summaries of relevant policy updates affecting radiopharmaceutical sourcing and cost recovery, and clinical context describing where the add‑on applies within nuclear medicine service lines. The publication outlines typical sites of service and operational considerations for billing but does not provide clinical recommendations. Data not available in the input is noted where applicable.
Billing Code Overview
HCPCS Level II code C9176 denotes Tc-99m derived from domestically produced non‑HEU Mo‑99 (minimum 50 percent), full cost recovery add‑on, per study dose. This code is intended to represent an add‑on supply component for nuclear medicine studies where technetium‑99m sourced from non‑highly enriched uranium molybdenum‑99 is used and a full cost recovery adjustment is applied on a per‑study‑dose basis.
Service Type: Nuclear medicine radiopharmaceutical add‑on.
Typical Site of Service: Hospital outpatient departments, hospital inpatient nuclear medicine departments, and freestanding imaging centers that perform diagnostic or therapeutic nuclear medicine studies.
Data not available in the input.
Clinical & Coding Specifications
Clinical Context
A typical patient is an adult undergoing a diagnostic nuclear medicine study requiring technetium-99m (Tc-99m) radiopharmaceutical labeled material. The facility has procured Tc-99m produced from domestically sourced, non-HEU molybdenum-99 (Mo-99) and bills an add-on charge for full cost recovery per study dose under C9176. The patient is referred from outpatient nuclear medicine, cardiology, oncology, or orthopedics for imaging such as bone scan, renal scan, hepatobiliary study, or myocardial perfusion imaging.
Workflow:
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Patient scheduled at an outpatient imaging center or hospital nuclear medicine department.
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Radiopharmacy verifies availability of domestically produced non-HEU Mo-99–derived
Tc-99mand prepares the study dose per routine sterile compounding and radiolabeling protocols. -
Patient arrives, identity and indications are confirmed; intravenous access or oral/voiding instructions are performed as appropriate for the specific scan.
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Radiopharmacist documents lot numbers, activity, and
C9176is added to billing as the per study dose add-on for the higher-cost domestically derived Tc-99m. -
Nuclear medicine technologist administers the
Tc-99mradiopharmaceutical; imaging is performed per protocol (timing, camera acquisition, SPECT/SPECT-CT or planar as indicated). -
Images are interpreted by a nuclear medicine physician or radiologist; results documented and reported to the referring clinician.