FDA NDC Directory · JSON-LD · Markdown

PRAVASTATIN SODIUM

NDC 82009-007 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerQuallent
Marketing categoryAbbreviated NDA (generic) · App ANDA076341
Dosage form / routeTABLET · ORAL
Active ingredientsPRAVASTATIN SODIUM (40 mg/1)
Marketing started20211203
Package count2

External sources

Source: openFDA. Public-domain (CC0).