Cefprozil - 65862-069-30 - (Cefprozil)

Alphabetical Index


Drug Information of Cefprozil

Product NDC: 65862-069
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: 65862-069
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065340
Marketing Category: ANDA
Start Marketing Date: 20070524

Package Information of Cefprozil

Package NDC: 65862-069-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (65862-069-30)

NDC Information of Cefprozil

NDC Code 65862-069-30
Proprietary Name Cefprozil
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (65862-069-30)
Product NDC 65862-069
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefprozil
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070524
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name CEFPROZIL
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Cefprozil


General Information