Cefprozil - 16714-208-01 - (Cefprozil)

Alphabetical Index


Drug Information of Cefprozil

Product NDC: 16714-208
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: 16714-208
Labeler Name: Northstar Rx LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065267
Marketing Category: ANDA
Start Marketing Date: 20070723

Package Information of Cefprozil

Package NDC: 16714-208-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16714-208-01)

NDC Information of Cefprozil

NDC Code 16714-208-01
Proprietary Name Cefprozil
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16714-208-01)
Product NDC 16714-208
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefprozil
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070723
Marketing Category Name ANDA
Labeler Name Northstar Rx LLC
Substance Name CEFPROZIL
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Cefprozil


General Information