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Omnaris
Omnaris - 63402-701-02 - (ciclesonide)
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: | 63402-701-02 |
| Package Description: | 1 POUCH in 1 CARTON (63402-701-02) > 1 BOTTLE, SPRAY in 1 POUCH > 60 SPRAY in 1 BOTTLE, SPRAY |
NDC Information of Omnaris
| NDC Code | 63402-701-02 |
| Proprietary Name | Omnaris |
| Package Description | 1 POUCH in 1 CARTON (63402-701-02) > 1 BOTTLE, SPRAY in 1 POUCH > 60 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 |
