United States · FDA National Drug Code directory
Boncresa
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 70121-2702_ea835cc4-6151-4b2e-ad69-3b2c6d32b078
- Product NDC
- 70121-2702
- Form
- INJECTION, SOLUTION
- Composition / generic term
- denosumab-mobz
- Labeler
- Amneal Pharmaceuticals LLC
- Marketing category
- BLA
- Marketing start / end (source format)
- 20251223
- Source listing expiry
- 20261231
Source-listed ingredients
- DENOSUMAB — 60 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 SYRINGE in 1 CARTON (70121-2702-1) / 1 mL in 1 SYRINGE · 70121-2702-1
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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