FDA NDC Directory · JSON-LD · Markdown

Pravastatin Sodium

NDC 0480-7270 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerTeva Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077793
Dosage form / routeTABLET · ORAL
Active ingredientsPRAVASTATIN SODIUM (80 mg/1)
Marketing started20230209
Package count2

External sources

Source: openFDA. Public-domain (CC0).