FDA NDC Directory · JSON-LD · Markdown

Cefprozil

NDC 67877-243 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA090857
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCEFPROZIL (500 mg/1)
Marketing started20250120
Package count1

External sources

Source: openFDA. Public-domain (CC0).