Cefadroxil - 21695-427-20 - (Cefadroxil)

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Drug Information of Cefadroxil

Product NDC: 21695-427
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: 21695-427
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065311
Marketing Category: ANDA
Start Marketing Date: 20060207

Package Information of Cefadroxil

Package NDC: 21695-427-20
Package Description: 20 CAPSULE in 1 BOTTLE (21695-427-20)

NDC Information of Cefadroxil

NDC Code 21695-427-20
Proprietary Name Cefadroxil
Package Description 20 CAPSULE in 1 BOTTLE (21695-427-20)
Product NDC 21695-427
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefadroxil
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20060207
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name CEFADROXIL
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Cefadroxil


General Information