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:
