FDA NDC Directory · JSON-LD · Markdown

Alendronate Sodium

NDC 0115-1678 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmneal Pharmaceuticals of New York LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA075710
Dosage form / routeTABLET · ORAL
Active ingredientsALENDRONATE SODIUM (10 mg/1)
Marketing started20080206
Package count2

External sources

Source: openFDA. Public-domain (CC0).