Armodafinil (Actavis Pharma, Inc.)
Welcome to the PulseAid listing for the Armodafinil drug offered from Actavis Pharma, 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: | Actavis Pharma, Inc. |
NON-PROPRIETARY NAME: | Armodafinil |
SUBSTANCE NAME: | ARMODAFINIL |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET |
MARKETING CATEGORY NAME: | NDA AUTHORIZED GENERIC |
START MARKETING DATE: | 2016-06-01 |
END MARKETING DATE: | 0000-00-00 |
Armodafinil HUMAN PRESCRIPTION DRUG Details:
Item Description | Armodafinil from Actavis Pharma, Inc. |
LABELER NAME: | Actavis Pharma, Inc. |
DEA SCHEDULE: | CIV
|
ACTIVE STRENGTH: | 200(mg/1) |
START MARKETING DATE: | 2016-06-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0591-3856_cfa0ae8e-1c94-42e8-a19c-7278cc5cf634 |
PRODUCT NDC: | 0591-3856 |
APPLICATION NUMBER: | NDA021875 |
Other ARMODAFINIL Pharmaceutical Manufacturers / Labelers: