Cefdinir

Product NDC
68071-3609
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Cefdinir
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA065259
Marketing category
ANDA
Substance
CEFDINIR
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
68071-3609-660 mL in 1 BOTTLE (68071-3609-6) 2024-06-25NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Cefdinir for Oral Suspension USPNuCare Pharmaceuticals,Inc.2024-06-25HUMAN PRESCRIPTION DRUG LABEL1