FDA NDC Directory · JSON-LD · Markdown

CEFDINIR

NDC 72189-259 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerDIRECT RX
Marketing categoryAbbreviated NDA (generic) · App ANDA210534
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsCEFDINIR (250 mg/5mL)
Marketing started20210913
Package count1

External sources

Source: openFDA. Public-domain (CC0).