FDA NDC Directory · JSON-LD · Markdown

BOMYNTRA

NDC 65219-672 · HUMAN PRESCRIPTION DRUG · INJECTION

Generic nameDenosumab
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryBiologic License Application · App BLA761398
Dosage form / routeINJECTION · SUBCUTANEOUS
Active ingredientsDENOSUMAB (70 mg/mL)
Marketing started20250630
Package count1

External sources

Source: openFDA. Public-domain (CC0).