FDA NDC Directory · JSON-LD · Markdown

CEFPROZIL

NDC 68180-404 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerLupin Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA065276
Dosage form / routeTABLET · ORAL
Active ingredientsCEFPROZIL (500 mg/1)
Marketing started20051201
Package count1

External sources

Source: openFDA. Public-domain (CC0).