CEFPROZIL - 64679-713-01 - (CEFPROZIL)

Alphabetical Index


Drug Information of CEFPROZIL

Product NDC: 64679-713
Proprietary Name: CEFPROZIL
Non Proprietary Name: CEFPROZIL
Active Ingredient(s): 500    mg/1 & nbsp;   CEFPROZIL
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of CEFPROZIL

Product NDC: 64679-713
Labeler Name: Wockhardt USA LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065428
Marketing Category: ANDA
Start Marketing Date: 20070615

Package Information of CEFPROZIL

Package NDC: 64679-713-01
Package Description: 50 TABLET, FILM COATED in 1 BOTTLE (64679-713-01)

NDC Information of CEFPROZIL

NDC Code 64679-713-01
Proprietary Name CEFPROZIL
Package Description 50 TABLET, FILM COATED in 1 BOTTLE (64679-713-01)
Product NDC 64679-713
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CEFPROZIL
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070615
Marketing Category Name ANDA
Labeler Name Wockhardt USA LLC.
Substance Name CEFPROZIL
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of CEFPROZIL


General Information