Cefadroxil - 0093-4059-53 - (Cefadroxil)

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Drug Information of Cefadroxil

Product NDC: 0093-4059
Proprietary Name: Cefadroxil
Non Proprietary Name: Cefadroxil
Active Ingredient(s): 1000    mg/1 & nbsp;   Cefadroxil
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Cefadroxil

Product NDC: 0093-4059
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062774
Marketing Category: ANDA
Start Marketing Date: 20070131

Package Information of Cefadroxil

Package NDC: 0093-4059-53
Package Description: 50 TABLET in 1 BOTTLE (0093-4059-53)

NDC Information of Cefadroxil

NDC Code 0093-4059-53
Proprietary Name Cefadroxil
Package Description 50 TABLET in 1 BOTTLE (0093-4059-53)
Product NDC 0093-4059
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefadroxil
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070131
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name CEFADROXIL
Strength Number 1000
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefadroxil


General Information