Omnaris - 63402-701-01 - (ciclesonide)

Alphabetical Index


Drug Information of Omnaris

Product NDC: 63402-701
Proprietary Name: Omnaris
Non Proprietary Name: ciclesonide
Active Ingredient(s): 50    ug/1 & nbsp;   ciclesonide
Administration Route(s): NASAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of Omnaris

Product NDC: 63402-701
Labeler Name: Sunovion Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022004
Marketing Category: NDA
Start Marketing Date: 20080301

Package Information of Omnaris

Package NDC: 63402-701-01
Package Description: 1 POUCH in 1 CARTON (63402-701-01) > 1 BOTTLE, SPRAY in 1 POUCH > 120 SPRAY in 1 BOTTLE, SPRAY

NDC Information of Omnaris

NDC Code 63402-701-01
Proprietary Name Omnaris
Package Description 1 POUCH in 1 CARTON (63402-701-01) > 1 BOTTLE, SPRAY in 1 POUCH > 120 SPRAY in 1 BOTTLE, SPRAY
Product NDC 63402-701
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ciclesonide
Dosage Form Name SPRAY
Route Name NASAL
Start Marketing Date 20080301
Marketing Category Name NDA
Labeler Name Sunovion Pharmaceuticals Inc.
Substance Name CICLESONIDE
Strength Number 50
Strength Unit ug/1
Pharmaceutical Classes

Complete Information of Omnaris


General Information