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: