FDA NDC Directory · JSON-LD · Markdown

Pravastatin Sodium

NDC 70518-2505 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA076056
Dosage form / routeTABLET · ORAL
Active ingredientsPRAVASTATIN SODIUM (40 mg/1)
Marketing started20191224
Marketing ended20260930
Package count0

External sources

Source: openFDA. Public-domain (CC0).