FDA NDC Directory · JSON-LD · Markdown

Pravastatin Sodium

NDC 68788-8871 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076056
Dosage form / routeTABLET · ORAL
Active ingredientsPRAVASTATIN SODIUM (20 mg/1)
Marketing started20250430
Package count3

External sources

Source: openFDA. Public-domain (CC0).