Provigil (Cephalon, Incorporated)
Welcome to the PulseAid listing for the Provigil drug offered from Cephalon, Incorporated. This Central Nervous System Stimulation [PE],Increased Sympathetic Activity [PE],Sympathomimetic-like Agent [EPC] 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: | Cephalon, Incorporated |
NON-PROPRIETARY NAME: | Modafinil |
SUBSTANCE NAME: | MODAFINIL |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Central Nervous System Stimulation [PE],Increased Sympathetic Activity [PE],Sympathomimetic-like Agent [EPC] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 1999-02-15 |
END MARKETING DATE: | 0000-00-00 |
Provigil HUMAN PRESCRIPTION DRUG Details:
Item Description | Provigil from Cephalon, Incorporated |
LABELER NAME: | Cephalon, Incorporated |
DEA SCHEDULE: | CIV
|
ACTIVE STRENGTH: | 100(mg/1) |
START MARKETING DATE: | 1999-02-15 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 63459-101_9b5ee9cb-87aa-4605-a8c3-c57bb956abae |
PRODUCT NDC: | 63459-101 |
APPLICATION NUMBER: | NDA020717 |
Other MODAFINIL Pharmaceutical Manufacturers / Labelers: