DUREZOL - 54868-6296-0 - (DUREZOL)

Alphabetical Index


Drug Information of DUREZOL

Product NDC: 54868-6296
Proprietary Name: DUREZOL
Non Proprietary Name: DUREZOL
Active Ingredient(s): .5    mg/mL & nbsp;   DUREZOL
Administration Route(s): OPHTHALMIC
Dosage Form(s): EMULSION
Coding System: National Drug Codes(NDC)

Labeler Information of DUREZOL

Product NDC: 54868-6296
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022212
Marketing Category: NDA
Start Marketing Date: 20110829

Package Information of DUREZOL

Package NDC: 54868-6296-0
Package Description: 1 BOTTLE in 1 CARTON (54868-6296-0) > 5 mL in 1 BOTTLE

NDC Information of DUREZOL

NDC Code 54868-6296-0
Proprietary Name DUREZOL
Package Description 1 BOTTLE in 1 CARTON (54868-6296-0) > 5 mL in 1 BOTTLE
Product NDC 54868-6296
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DUREZOL
Dosage Form Name EMULSION
Route Name OPHTHALMIC
Start Marketing Date 20110829
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name DIFLUPREDNATE
Strength Number .5
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of DUREZOL


General Information