FDA NDC Directory · JSON-LD · Markdown

Alendronate Sodium

NDC 0054-0282 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090520
Dosage form / routeSOLUTION · ORAL
Active ingredientsALENDRONATE SODIUM (70 mg/75mL)
Marketing started20201030
Package count1

External sources

Source: openFDA. Public-domain (CC0).