Cefprozil - 0093-1075-78 - (Cefprozil)

Alphabetical Index


Drug Information of Cefprozil

Product NDC: 0093-1075
Proprietary Name: Cefprozil
Non Proprietary Name: Cefprozil
Active Ingredient(s): 125    mg/5mL & nbsp;   Cefprozil
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Cefprozil

Product NDC: 0093-1075
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065236
Marketing Category: ANDA
Start Marketing Date: 20060304

Package Information of Cefprozil

Package NDC: 0093-1075-78
Package Description: 75 mL in 1 BOTTLE (0093-1075-78)

NDC Information of Cefprozil

NDC Code 0093-1075-78
Proprietary Name Cefprozil
Package Description 75 mL in 1 BOTTLE (0093-1075-78)
Product NDC 0093-1075
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefprozil
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20060304
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name CEFPROZIL
Strength Number 125
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Cefprozil


General Information