FDA NDC Directory · JSON-LD · Markdown

PRAVASTATIN SODIUM

NDC 0615-8619 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
Marketing categoryAbbreviated NDA (generic) · App ANDA076341
Dosage form / routeTABLET · ORAL
Active ingredientsPRAVASTATIN SODIUM (20 mg/1)
Marketing started20110718
Package count2

External sources

Source: openFDA. Public-domain (CC0).