FDA NDC Directory · JSON-LD · Markdown

Pravastatin Sodium

NDC 0093-7201 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerTeva Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076056
Dosage form / routeTABLET · ORAL
Active ingredientsPRAVASTATIN SODIUM (20 mg/1)
Marketing started20060425
Marketing ended20261231
Package count2

External sources

Source: openFDA. Public-domain (CC0).