Cefdinir - 0093-4137-64 - (Cefdinir)

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Drug Information of Cefdinir

Product NDC: 0093-4137
Proprietary Name: Cefdinir
Non Proprietary Name: Cefdinir
Active Ingredient(s): 250    mg/5mL & nbsp;   Cefdinir
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Cefdinir

Product NDC: 0093-4137
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065332
Marketing Category: ANDA
Start Marketing Date: 20070508

Package Information of Cefdinir

Package NDC: 0093-4137-64
Package Description: 60 mL in 1 BOTTLE (0093-4137-64)

NDC Information of Cefdinir

NDC Code 0093-4137-64
Proprietary Name Cefdinir
Package Description 60 mL in 1 BOTTLE (0093-4137-64)
Product NDC 0093-4137
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefdinir
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20070508
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name CEFDINIR MONOHYDRATE
Strength Number 250
Strength Unit mg/5mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefdinir


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