FDA NDC Directory · JSON-LD · Markdown

CEFIXIME

NDC 68180-405 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerLupin Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA065129
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsCEFIXIME (100 mg/5mL)
Marketing started20150424
Package count1

External sources

Source: openFDA. Public-domain (CC0).