Cefprozil - 0093-1078-01 - (Cefprozil)

Alphabetical Index


Drug Information of Cefprozil

Product NDC: 0093-1078
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: 0093-1078
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065208
Marketing Category: ANDA
Start Marketing Date: 20051223

Package Information of Cefprozil

Package NDC: 0093-1078-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0093-1078-01)

NDC Information of Cefprozil

NDC Code 0093-1078-01
Proprietary Name Cefprozil
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0093-1078-01)
Product NDC 0093-1078
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefprozil
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20051223
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name CEFPROZIL
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Cefprozil


General Information