FDA NDC Directory · JSON-LD · Markdown

Pravastatin Sodium

NDC 71205-294 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA076056
Dosage form / routeTABLET · ORAL
Active ingredientsPRAVASTATIN SODIUM (40 mg/1)
Marketing started20060425
Package count3

External sources

Source: openFDA. Public-domain (CC0).