Dronabinol (Akorn, Inc.)
Welcome to the PulseAid listing for the Dronabinol drug offered from Akorn, Inc.. This Cannabinoid [EPC],Cannabinoids [Chemical/Ingredient] 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: | Akorn, Inc. |
NON-PROPRIETARY NAME: | Dronabinol |
SUBSTANCE NAME: | DRONABINOL |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Cannabinoid [EPC],Cannabinoids [Chemical/Ingredient] |
ROUTE: | ORAL |
DOSAGE FORM: | CAPSULE |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2014-06-20 |
END MARKETING DATE: | 0000-00-00 |
Dronabinol HUMAN PRESCRIPTION DRUG Details:
Item Description | Dronabinol from Akorn, Inc. |
LABELER NAME: | Akorn, Inc. |
DEA SCHEDULE: | CIII
|
ACTIVE STRENGTH: | 2.5(mg/1) |
START MARKETING DATE: | 2014-06-20 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 17478-761_25e42cf9-e32f-4bfc-862b-91c4238dca43 |
PRODUCT NDC: | 17478-761 |
APPLICATION NUMBER: | ANDA079217 |
Other DRONABINOL Pharmaceutical Manufacturers / Labelers: