FDA NDC Directory · JSON-LD · Markdown

Alendronate

NDC 10135-718 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameAlendronate sodium tablet
Labeler / ManufacturerMarlex Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090258
Dosage form / routeTABLET · ORAL
Active ingredientsALENDRONATE SODIUM (35 mg/1)
Marketing started20201201
Package count2

External sources

Source: openFDA. Public-domain (CC0).