Cefadroxil - 0781-2938-01 - (Cefadroxil)

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Drug Information of Cefadroxil

Product NDC: 0781-2938
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: 0781-2938
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062291
Marketing Category: ANDA
Start Marketing Date: 19800730

Package Information of Cefadroxil

Package NDC: 0781-2938-01
Package Description: 100 CAPSULE in 1 BOTTLE (0781-2938-01)

NDC Information of Cefadroxil

NDC Code 0781-2938-01
Proprietary Name Cefadroxil
Package Description 100 CAPSULE in 1 BOTTLE (0781-2938-01)
Product NDC 0781-2938
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefadroxil
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19800730
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name CEFADROXIL
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Cefadroxil


General Information