FDA NDC Directory · JSON-LD · Markdown

PRAVASTATIN SODIUM

NDC 60687-908 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA077987
Dosage form / routeTABLET · ORAL
Active ingredientsPRAVASTATIN SODIUM (40 mg/1)
Marketing started20250302
Marketing ended20270331
Package count1

External sources

Source: openFDA. Public-domain (CC0).