FDA NDC Directory · JSON-LD · Markdown

PRAVASTATIN SODIUM

NDC 68788-7009 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076341
Dosage form / routeTABLET · ORAL
Active ingredientsPRAVASTATIN SODIUM (40 mg/1)
Marketing started20220927
Package count6

External sources

Source: openFDA. Public-domain (CC0).