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NDC 0143-9166 · HUMAN PRESCRIPTION DRUG · INJECTION

Generic nameDenosumab-qbde
Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryBiologic License Application · App BLA761439
Dosage form / routeINJECTION · SUBCUTANEOUS
Active ingredientsDENOSUMAB (120 mg/1.7mL)
Marketing started20260108
Package count1

External sources

Source: openFDA. Public-domain (CC0).