Cefadroxil - 65862-084-01 - (Cefadroxil)

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Drug Information of Cefadroxil

Product NDC: 65862-084
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: 65862-084
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065349
Marketing Category: ANDA
Start Marketing Date: 20130425

Package Information of Cefadroxil

Package NDC: 65862-084-01
Package Description: 100 mL in 1 BOTTLE (65862-084-01)

NDC Information of Cefadroxil

NDC Code 65862-084-01
Proprietary Name Cefadroxil
Package Description 100 mL in 1 BOTTLE (65862-084-01)
Product NDC 65862-084
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefadroxil
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20130425
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name CEFADROXIL
Strength Number 500
Strength Unit mg/5mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefadroxil


General Information