FDA NDC Directory · JSON-LD · Markdown

cefdinir

NDC 68788-8115 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA210534
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsCEFDINIR (125 mg/5mL)
Marketing started20211207
Package count2

External sources

Source: openFDA. Public-domain (CC0).