Dexmethylphenidate Hydrochloride (Teva Pharmaceuticals USA, Inc.)
Welcome to the PulseAid listing for the Dexmethylphenidate Hydrochloride drug offered from Teva Pharmaceuticals USA, 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: | Teva Pharmaceuticals USA, 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: | TABLET |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2007-06-08 |
| END MARKETING DATE: | 0000-00-00 |
Dexmethylphenidate Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Dexmethylphenidate Hydrochloride from Teva Pharmaceuticals USA, Inc. |
| LABELER NAME: | Teva Pharmaceuticals USA, Inc. |
| DEA SCHEDULE: | CII
|
| ACTIVE STRENGTH: | 2.5(mg/1) |
| START MARKETING DATE: | 2007-06-08 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0093-5275_46e55d2b-8a15-4916-8fc8-b520c3ece570 |
| PRODUCT NDC: | 0093-5275 |
| APPLICATION NUMBER: | ANDA077107 |
Other DEXMETHYLPHENIDATE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
