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ALENDRONATE SODIUM

NDC 68071-3771 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameAlendronate sodium
Labeler / ManufacturerNuCare Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076768
Dosage form / routeTABLET · ORAL
Active ingredientsALENDRONATE SODIUM (70 mg/1)
Marketing started20080804
Package count1

External sources

Source: openFDA. Public-domain (CC0).