FDA NDC Directory · JSON-LD · Markdown

PRAVASTATIN SODIUM

NDC 51655-976 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA076341
Dosage form / routeTABLET · ORAL
Active ingredientsPRAVASTATIN SODIUM (80 mg/1)
Marketing started20220413
Package count1

External sources

Source: openFDA. Public-domain (CC0).