FDA NDC Directory · JSON-LD · Markdown

ALENDRONATE SODIUM

NDC 70518-1192 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameAlendronate sodium
Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA076768
Dosage form / routeTABLET · ORAL
Active ingredientsALENDRONATE SODIUM (35 mg/1)
Marketing started20180516
Package count1

External sources

Source: openFDA. Public-domain (CC0).