FDA NDC Directory · JSON-LD · Markdown

Enalapril Maleate

NDC 51672-4040 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerTaro Pharmaceuticals U.S.A., Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA075657
Dosage form / routeTABLET · ORAL
Active ingredientsENALAPRIL MALEATE (20 mg/1)
Marketing started20010123
Package count2

External sources

Source: openFDA. Public-domain (CC0).