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: