Armodafinil (Teva Pharmaceuticals USA, Inc.)
Welcome to the PulseAid listing for the Armodafinil drug offered from Teva Pharmaceuticals USA, 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: | Teva Pharmaceuticals USA, 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: | 2016-11-29 |
| END MARKETING DATE: | 0000-00-00 |
Armodafinil HUMAN PRESCRIPTION DRUG Details:
| Item Description | Armodafinil from Teva Pharmaceuticals USA, Inc. |
| LABELER NAME: | Teva Pharmaceuticals USA, Inc. |
| DEA SCHEDULE: | CIV
|
| ACTIVE STRENGTH: | 50(mg/1) |
| START MARKETING DATE: | 2016-11-29 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0093-3090_43e4648e-388b-4fa6-9f79-51f2cbe50978 |
| PRODUCT NDC: | 0093-3090 |
| APPLICATION NUMBER: | NDA021875 |
Other ARMODAFINIL Pharmaceutical Manufacturers / Labelers:
