FDA NDC Directory · JSON-LD · Markdown

PRAVASTATIN SODIUM

NDC 60505-1323 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerApotex Corp.
Marketing categoryAbbreviated NDA (generic) · App ANDA076341
Dosage form / routeTABLET · ORAL
Active ingredientsPRAVASTATIN SODIUM (80 mg/1)
Marketing started20110718
Package count5

External sources

Source: openFDA. Public-domain (CC0).