OZURDEX - 0023-3348-07 - (dexamethasone)

Alphabetical Index


Drug Information of OZURDEX

Product NDC: 0023-3348
Proprietary Name: OZURDEX
Non Proprietary Name: dexamethasone
Active Ingredient(s): .7    mg/1 & nbsp;   dexamethasone
Administration Route(s): INTRAVITREAL
Dosage Form(s): IMPLANT
Coding System: National Drug Codes(NDC)

Labeler Information of OZURDEX

Product NDC: 0023-3348
Labeler Name: Allergan, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022315
Marketing Category: NDA
Start Marketing Date: 20090901

Package Information of OZURDEX

Package NDC: 0023-3348-07
Package Description: 1 POUCH in 1 CARTON (0023-3348-07) > 1 IMPLANT in 1 POUCH

NDC Information of OZURDEX

NDC Code 0023-3348-07
Proprietary Name OZURDEX
Package Description 1 POUCH in 1 CARTON (0023-3348-07) > 1 IMPLANT in 1 POUCH
Product NDC 0023-3348
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name dexamethasone
Dosage Form Name IMPLANT
Route Name INTRAVITREAL
Start Marketing Date 20090901
Marketing Category Name NDA
Labeler Name Allergan, Inc.
Substance Name DEXAMETHASONE
Strength Number .7
Strength Unit mg/1
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of OZURDEX


General Information