Omnaris (Sunovion Pharmaceuticals Inc.)
Welcome to the PulseAid listing for the Omnaris drug offered from Sunovion Pharmaceuticals Inc.. This pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Sunovion Pharmaceuticals Inc. |
| NON-PROPRIETARY NAME: | ciclesonide |
| SUBSTANCE NAME: | CICLESONIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | NASAL |
| DOSAGE FORM: | SPRAY |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 2008-03-01 |
| END MARKETING DATE: | 0000-00-00 |
Omnaris HUMAN PRESCRIPTION DRUG Details:
| Item Description | Omnaris from Sunovion Pharmaceuticals Inc. |
| LABELER NAME: | Sunovion Pharmaceuticals Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 50(ug/1) |
| START MARKETING DATE: | 2008-03-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 63402-701_986679b3-44c9-40db-9a62-38ec354a5145 |
| PRODUCT NDC: | 63402-701 |
| APPLICATION NUMBER: | NDA022004 |
Other CICLESONIDE Pharmaceutical Manufacturers / Labelers:
