FDA NDC Directory · JSON-LD · Markdown

Pravastatin Sodium

NDC 69292-104 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmici Pharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077491
Dosage form / routeTABLET · ORAL
Active ingredientsPRAVASTATIN SODIUM (80 mg/1)
Marketing started20260519
Package count3

External sources

Source: openFDA. Public-domain (CC0).