FDA NDC Directory · JSON-LD · Markdown

Pravastatin Sodium

NDC 50090-6898 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerA-S Medication Solutions
Marketing categoryAbbreviated NDA (generic) · App ANDA076056
Dosage form / routeTABLET · ORAL
Active ingredientsPRAVASTATIN SODIUM (20 mg/1)
Marketing started20060425
Package count1

External sources

Source: openFDA. Public-domain (CC0).