FDA NDC Directory · JSON-LD · Markdown

CEFPROZIL

NDC 68180-401 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerLupin Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA065261
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsCEFPROZIL (125 mg/5mL)
Marketing started20051201
Package count1

External sources

Source: openFDA. Public-domain (CC0).