FDA NDC Directory · JSON-LD · Markdown

Pravastatin Sodium

NDC 55154-5370 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerCardinal Health 107, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA076056
Dosage form / routeTABLET · ORAL
Active ingredientsPRAVASTATIN SODIUM (40 mg/1)
Marketing started20120210
Marketing ended20260831
Package count1

External sources

Source: openFDA. Public-domain (CC0).