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PRAVASTATIN SODIUM

NDC 0615-8542 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
Marketing categoryAbbreviated NDA (generic) · App ANDA077987
Dosage form / routeTABLET · ORAL
Active ingredientsPRAVASTATIN SODIUM (80 mg/1)
Marketing started20240601
Marketing ended20261130
Package count1

External sources

Source: openFDA. Public-domain (CC0).