FDA NDC Directory · JSON-LD · Markdown

Pravastatin sodium

NDC 70377-048 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerBiocon Pharma Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209869
Dosage form / routeTABLET · ORAL
Active ingredientsPRAVASTATIN SODIUM (80 mg/1)
Marketing started20210201
Package count3

External sources

Source: openFDA. Public-domain (CC0).