Cefadroxil - 65862-085-50 - (Cefadroxil)

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Drug Information of Cefadroxil

Product NDC: 65862-085
Proprietary Name: Cefadroxil
Non Proprietary Name: Cefadroxil
Active Ingredient(s): 500    mg/1 & nbsp;   Cefadroxil
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Cefadroxil

Product NDC: 65862-085
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065352
Marketing Category: ANDA
Start Marketing Date: 20070125

Package Information of Cefadroxil

Package NDC: 65862-085-50
Package Description: 50 CAPSULE in 1 BOTTLE (65862-085-50)

NDC Information of Cefadroxil

NDC Code 65862-085-50
Proprietary Name Cefadroxil
Package Description 50 CAPSULE in 1 BOTTLE (65862-085-50)
Product NDC 65862-085
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefadroxil
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20070125
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name CEFADROXIL
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefadroxil


General Information