CEFPROZIL - 68180-402-02 - (CEFPROZIL)

Alphabetical Index


Drug Information of CEFPROZIL

Product NDC: 68180-402
Proprietary Name: CEFPROZIL
Non Proprietary Name: CEFPROZIL
Active Ingredient(s): 250    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: 68180-402
Labeler Name: LUPIN PHARMACEUTICALS INC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065261
Marketing Category: ANDA
Start Marketing Date: 20051201

Package Information of CEFPROZIL

Package NDC: 68180-402-02
Package Description: 75 mL in 1 BOTTLE (68180-402-02)

NDC Information of CEFPROZIL

NDC Code 68180-402-02
Proprietary Name CEFPROZIL
Package Description 75 mL in 1 BOTTLE (68180-402-02)
Product NDC 68180-402
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CEFPROZIL
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20051201
Marketing Category Name ANDA
Labeler Name LUPIN PHARMACEUTICALS INC
Substance Name CEFPROZIL
Strength Number 250
Strength Unit mg/5mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of CEFPROZIL


General Information