CEFPROZIL - 68180-404-02 - (CEFPROZIL)

Alphabetical Index


Drug Information of CEFPROZIL

Product NDC: 68180-404
Proprietary Name: CEFPROZIL
Non Proprietary Name: CEFPROZIL
Active Ingredient(s): 500    mg/1 & nbsp;   CEFPROZIL
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of CEFPROZIL

Product NDC: 68180-404
Labeler Name: Lupin Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065276
Marketing Category: ANDA
Start Marketing Date: 20051201

Package Information of CEFPROZIL

Package NDC: 68180-404-02
Package Description: 100 TABLET in 1 BOTTLE (68180-404-02)

NDC Information of CEFPROZIL

NDC Code 68180-404-02
Proprietary Name CEFPROZIL
Package Description 100 TABLET in 1 BOTTLE (68180-404-02)
Product NDC 68180-404
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CEFPROZIL
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20051201
Marketing Category Name ANDA
Labeler Name Lupin Pharmaceuticals, Inc.
Substance Name CEFPROZIL
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of CEFPROZIL


General Information