Armodafinil (Breckenridge Pharmaceutical, Inc.)
Welcome to the PulseAid listing for the Armodafinil drug offered from Breckenridge Pharmaceutical, 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: | Breckenridge Pharmaceutical, Inc. |
| NON-PROPRIETARY NAME: | Armodafinil |
| SUBSTANCE NAME: | ARMODAFINIL |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2016-11-28 |
| END MARKETING DATE: | 0000-00-00 |
Armodafinil HUMAN PRESCRIPTION DRUG Details:
| Item Description | Armodafinil from Breckenridge Pharmaceutical, Inc. |
| LABELER NAME: | Breckenridge Pharmaceutical, Inc. |
| DEA SCHEDULE: | CIV
|
| ACTIVE STRENGTH: | 50(mg/1) |
| START MARKETING DATE: | 2016-11-28 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 51991-322_0d1a6384-50ec-4488-9a91-470c4e75f32a |
| PRODUCT NDC: | 51991-322 |
| APPLICATION NUMBER: | ANDA202768 |
Other ARMODAFINIL Pharmaceutical Manufacturers / Labelers:
