FDA NDC Directory · JSON-LD · Markdown

Lovastatin

NDC 68180-468 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namelovastatin
Labeler / ManufacturerLupin Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078296
Dosage form / routeTABLET · ORAL
Active ingredientsLOVASTATIN (20 mg/1)
Marketing started20071101
Package count4

External sources

Source: openFDA. Public-domain (CC0).