Cefadroxil - 0093-4181-73 - (Cefadroxil)

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Drug Information of Cefadroxil

Product NDC: 0093-4181
Proprietary Name: Cefadroxil
Non Proprietary Name: Cefadroxil
Active Ingredient(s): 500    mg/5mL & nbsp;   Cefadroxil
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Cefadroxil

Product NDC: 0093-4181
Labeler Name: TEVA Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065278
Marketing Category: ANDA
Start Marketing Date: 20100202

Package Information of Cefadroxil

Package NDC: 0093-4181-73
Package Description: 100 mL in 1 BOTTLE (0093-4181-73)

NDC Information of Cefadroxil

NDC Code 0093-4181-73
Proprietary Name Cefadroxil
Package Description 100 mL in 1 BOTTLE (0093-4181-73)
Product NDC 0093-4181
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefadroxil
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20100202
Marketing Category Name ANDA
Labeler Name TEVA Pharmaceuticals USA Inc
Substance Name CEFADROXIL
Strength Number 500
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Cefadroxil


General Information