FDA NDC Directory · JSON-LD · Markdown

PRAVASTATIN SODIUM

NDC 71610-877 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAphena Pharma Solutions - Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA209869
Dosage form / routeTABLET · ORAL
Active ingredientsPRAVASTATIN SODIUM (80 mg/1)
Marketing started20180413
Package count4

External sources

Source: openFDA. Public-domain (CC0).