Prescription drug · BLA
Boncresa (Denosumab-mobz) NDC 70121-2702
Denosumab 60 mg/mL · Injection, Solution · Subcutaneous · Amneal Pharmaceuticals LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70121-2702-1 | 70121270201 | 1 SYRINGE in 1 CARTON (70121-2702-1) / 1 mL in 1 SYRINGEMarketed from Dec 23, 2025 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Boncresa
- Generic name (nonproprietary)
- denosumab-mobz
- Active ingredients
- Denosumab — 60 mg/mL
- Dosage form
- Injection, Solution
- Route
- Subcutaneous
- Labeler
- Amneal Pharmaceuticals LLCNDC labeler code 70121
- Product type
- Prescription drug
- Marketing category
- BLA — Biologics License ApplicationApplication BLA 761456
- Marketing start
- Listing expires
- Other FDA classes
- RANK Ligand Blocking Activity (Mechanism)
- Identifiers
- Product ID 70121-2702_ea835cc4-6151-4b2e-ad69-3b2c6d32b078SPL ID ea835cc4-6151-4b2e-ad69-3b2c6d32b078SPL set ID 29140df2-24a3-4a6f-a8e3-065521448d61RxCUI 2729312, 2729319UNII 4EQZ6YO2HIUPC 0370121270218
- Pharmacologic class
- RANK Ligand Inhibitor
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeMed-Code curated
J0897 — Injection, denosumab, 1 mg
Billing unit: 1 mg. Units on the claim = dose given ÷ 1 mg.
Denosumab biosimilars have their own HCPCS codes.
- Administration
Drug administration (CPT 96360–96549)
When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.
- NDC on a medical claim
N470121270201followed by a unit qualifier and the quantityPackage 70121-2702-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective . This label includes a boxed warning.
Indications (excerpt from the label)
Boncresa is a RANK ligand (RANKL) inhibitor indicated for treatment: of postmenopausal women with osteoporosis at high risk for fracture (1.1) to increase bone mass in men with osteoporosis at high risk for fracture (1.2) of glucocorticoid-induced osteoporosis in men and women at high risk for fracture (1.3) to increase bone mass in men at high risk for fracture receiving androgen deprivation therapy for nonmetastatic prostate cancer (1.4) to increase bone mass in women at high risk for fracture receiving adjuvant aromatase inhibitor therapy for breast cancer (1.5) 1.1 Treatment of Postmenopausal Women with Osteoporosis at High Risk for Fracture Boncresa is indicated for the treatment of pos…
Excerpt only. Read the full label for complete information.
About NDC 70121-2702
- What is NDC 70121-2702?
- 70121-2702 is the product NDC for Boncresa (denosumab-mobz), Denosumab 60 mg/mL injection, solution, listed with the FDA by Amneal Pharmaceuticals LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Boncresa (Denosumab-mobz).
- What is the active ingredient?
- Denosumab.
- Who is the labeler?
- Amneal Pharmaceuticals LLC, NDC labeler code 70121. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Boncresa?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Yes: J0897, Injection, denosumab, 1 mg. See Billing references above.