Cefprozil - 16714-215-03 - (Cefprozil)

Alphabetical Index


Drug Information of Cefprozil

Product NDC: 16714-215
Proprietary Name: Cefprozil
Non Proprietary Name: Cefprozil
Active Ingredient(s): 125    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: 16714-215
Labeler Name: Northstar Rx LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065284
Marketing Category: ANDA
Start Marketing Date: 20070723

Package Information of Cefprozil

Package NDC: 16714-215-03
Package Description: 100 mL in 1 BOTTLE (16714-215-03)

NDC Information of Cefprozil

NDC Code 16714-215-03
Proprietary Name Cefprozil
Package Description 100 mL in 1 BOTTLE (16714-215-03)
Product NDC 16714-215
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefprozil
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20070723
Marketing Category Name ANDA
Labeler Name Northstar Rx LLC
Substance Name CEFPROZIL
Strength Number 125
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Cefprozil


General Information