Cefprozil - 0781-6202-91 - (Cefprozil)

Alphabetical Index


Drug Information of Cefprozil

Product NDC: 0781-6202
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: 0781-6202
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065257
Marketing Category: ANDA
Start Marketing Date: 20051205

Package Information of Cefprozil

Package NDC: 0781-6202-91
Package Description: 50 mL in 1 BOTTLE (0781-6202-91)

NDC Information of Cefprozil

NDC Code 0781-6202-91
Proprietary Name Cefprozil
Package Description 50 mL in 1 BOTTLE (0781-6202-91)
Product NDC 0781-6202
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefprozil
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20051205
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name CEFPROZIL
Strength Number 125
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Cefprozil


General Information