Zetonna (Sunovion Pharmaceuticals Inc.)


Welcome to the PulseAid listing for the Zetonna 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: AEROSOL, METERED
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2012-07-30
END MARKETING DATE: 0000-00-00


Zetonna HUMAN PRESCRIPTION DRUG Details:

Item DescriptionZetonna from Sunovion Pharmaceuticals Inc.
LABELER NAME: Sunovion Pharmaceuticals Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 37(ug/1)
START MARKETING DATE: 2012-07-30
END MARKETING DATE: 0000-00-00
PRODUCT ID: 63402-737_1f501927-7ef1-48d8-ade5-7fc7006e0db1
PRODUCT NDC: 63402-737
APPLICATION NUMBER: NDA202129

Other CICLESONIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Physicians Total Care, Inc.Alvesco
Sunovion Pharmaceuticals Inc.Omnaris