Cefprozil - 54569-6195-0 - (Cefprozil)

Alphabetical Index


Drug Information of Cefprozil

Product NDC: 54569-6195
Proprietary Name: Cefprozil
Non Proprietary Name: Cefprozil
Active Ingredient(s): 500    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: 54569-6195
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065267
Marketing Category: ANDA
Start Marketing Date: 20070723

Package Information of Cefprozil

Package NDC: 54569-6195-0
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54569-6195-0)

NDC Information of Cefprozil

NDC Code 54569-6195-0
Proprietary Name Cefprozil
Package Description 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54569-6195-0)
Product NDC 54569-6195
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 A-S Medication Solutions LLC
Substance Name CEFPROZIL
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Cefprozil


General Information