FDA NDC Directory · JSON-LD · Markdown

PRAVASTATIN SODIUM

NDC 50090-6826 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerA-S Medication Solutions
Marketing categoryAbbreviated NDA (generic) · App ANDA076341
Dosage form / routeTABLET · ORAL
Active ingredientsPRAVASTATIN SODIUM (40 mg/1)
Marketing started20110718
Package count1

External sources

Source: openFDA. Public-domain (CC0).