Cefadroxil - 54868-3742-3 - (cefadroxil hemihydrate)

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Drug Information of Cefadroxil

Product NDC: 54868-3742
Proprietary Name: Cefadroxil
Non Proprietary Name: cefadroxil hemihydrate
Active Ingredient(s): 500    mg/1 & nbsp;   cefadroxil hemihydrate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Cefadroxil

Product NDC: 54868-3742
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065015
Marketing Category: ANDA
Start Marketing Date: 19960423

Package Information of Cefadroxil

Package NDC: 54868-3742-3
Package Description: 10 CAPSULE in 1 BOTTLE (54868-3742-3)

NDC Information of Cefadroxil

NDC Code 54868-3742-3
Proprietary Name Cefadroxil
Package Description 10 CAPSULE in 1 BOTTLE (54868-3742-3)
Product NDC 54868-3742
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cefadroxil hemihydrate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19960423
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name CEFADROXIL HEMIHYDRATE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Cefadroxil


General Information