Aptiom (Sunovion Pharmaceuticals Inc.)


Welcome to the PulseAid listing for the Aptiom drug offered from Sunovion Pharmaceuticals Inc.. This Decreased Central Nervous System Disorganized Electrical Activity [PE],Cytochrome P450 3A4 Inducers [MoA],Cytochrome P450 2C19 Inhibitors [MoA] 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: ESLICARBAZEPINE ACETATE
SUBSTANCE NAME: ESLICARBAZEPINE ACETATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Decreased Central Nervous System Disorganized Electrical Activity [PE],Cytochrome P450 3A4 Inducers [MoA],Cytochrome P450 2C19 Inhibitors [MoA]
ROUTE: ORAL
DOSAGE FORM: TABLET
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2014-04-07
END MARKETING DATE: 0000-00-00


Aptiom HUMAN PRESCRIPTION DRUG Details:

Item DescriptionAptiom from Sunovion Pharmaceuticals Inc.
LABELER NAME: Sunovion Pharmaceuticals Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 200(mg/1)
START MARKETING DATE: 2014-04-07
END MARKETING DATE: 0000-00-00
PRODUCT ID: 63402-202_dbde4c7c-e9c4-4490-8b50-c682bcc0368b
PRODUCT NDC: 63402-202
APPLICATION NUMBER: NDA022416

Other ESLICARBAZEPINE ACETATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Sunovion Pharmaceuticals Inc.Aptiom