Dexmethylphenidate Hydrochloride (Actavis Pharma, Inc.)
Welcome to the PulseAid listing for the Dexmethylphenidate Hydrochloride drug offered from Actavis Pharma, Inc.. This Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE] 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: | Actavis Pharma, Inc. |
| NON-PROPRIETARY NAME: | Dexmethylphenidate Hydrochloride |
| SUBSTANCE NAME: | DEXMETHYLPHENIDATE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE] |
| ROUTE: | ORAL |
| DOSAGE FORM: | CAPSULE, EXTENDED RELEASE |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2014-12-01 |
| END MARKETING DATE: | 2018-02-08 |
Dexmethylphenidate Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Dexmethylphenidate Hydrochloride from Actavis Pharma, Inc. |
| LABELER NAME: | Actavis Pharma, Inc. |
| DEA SCHEDULE: | CII
|
| ACTIVE STRENGTH: | 15(mg/1) |
| START MARKETING DATE: | 2014-12-01 |
| END MARKETING DATE: | 2018-02-08 |
| PRODUCT ID: | 45963-806_713c4833-e483-4962-9b68-10eccc8b8c12 |
| PRODUCT NDC: | 45963-806 |
| APPLICATION NUMBER: | ANDA079108 |
Other DEXMETHYLPHENIDATE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
