FDA NDC Directory · JSON-LD · Markdown

PRAVASTATIN SODIUM

NDC 68180-487 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerLupin Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077917
Dosage form / routeTABLET · ORAL
Active ingredientsPRAVASTATIN SODIUM (40 mg/1)
Marketing started20080724
Package count0

External sources

Source: openFDA. Public-domain (CC0).