FDA NDC Directory · JSON-LD · Markdown

Alendronate Sodium

NDC 64980-342 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090124
Dosage form / routeTABLET · ORAL
Active ingredientsALENDRONATE SODIUM (70 mg/1)
Marketing started20080804
Package count3

External sources

Source: openFDA. Public-domain (CC0).