FDA NDC Directory · JSON-LD · Markdown

Cefdinir

NDC 68071-4970 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA065473
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsCEFDINIR (125 mg/5mL)
Marketing started20071214
Package count1

External sources

Source: openFDA. Public-domain (CC0).