VIIBRYD (Allergan, Inc.)
Welcome to the PulseAid listing for the VIIBRYD drug offered from Allergan, 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: | Allergan, Inc. |
NON-PROPRIETARY NAME: | vilazodone hydrochloride |
SUBSTANCE NAME: | VILAZODONE HYDROCHLORIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2011-04-29 |
END MARKETING DATE: | 0000-00-00 |
VIIBRYD HUMAN PRESCRIPTION DRUG Details:
Item Description | VIIBRYD from Allergan, Inc. |
LABELER NAME: | Allergan, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 10(mg/1) |
START MARKETING DATE: | 2011-04-29 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0456-1110_f180b475-4aa3-4c3d-965e-c7e2e41ad8bb |
PRODUCT NDC: | 0456-1110 |
APPLICATION NUMBER: | NDA022567 |
Other VILAZODONE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: