Cefprozil - 60505-2532-5 - (Cefprozil)

Alphabetical Index


Drug Information of Cefprozil

Product NDC: 60505-2532
Proprietary Name: Cefprozil
Non Proprietary Name: Cefprozil
Active Ingredient(s): 250    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: 60505-2532
Labeler Name: Apotex Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065327
Marketing Category: ANDA
Start Marketing Date: 20080509

Package Information of Cefprozil

Package NDC: 60505-2532-5
Package Description: 50 TABLET, FILM COATED in 1 BOTTLE (60505-2532-5)

NDC Information of Cefprozil

NDC Code 60505-2532-5
Proprietary Name Cefprozil
Package Description 50 TABLET, FILM COATED in 1 BOTTLE (60505-2532-5)
Product NDC 60505-2532
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefprozil
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080509
Marketing Category Name ANDA
Labeler Name Apotex Corp
Substance Name CEFPROZIL
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Cefprozil


General Information