Dexmethylphenidate hydrochloride (Sun Pharmaceutical Industries, Inc.)
Welcome to the PulseAid listing for the Dexmethylphenidate hydrochloride drug offered from Sun Pharmaceutical Industries, 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: | Sun Pharmaceutical Industries, 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: | 2013-09-26 |
| END MARKETING DATE: | 0000-00-00 |
Dexmethylphenidate hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Dexmethylphenidate hydrochloride from Sun Pharmaceutical Industries, Inc. |
| LABELER NAME: | Sun Pharmaceutical Industries, Inc. |
| DEA SCHEDULE: | CII
|
| ACTIVE STRENGTH: | 2.5(mg/1) |
| START MARKETING DATE: | 2013-09-26 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 57664-376_68698e79-4e01-4935-b298-c64876bf40ec |
| PRODUCT NDC: | 57664-376 |
| APPLICATION NUMBER: | ANDA201231 |
Other DEXMETHYLPHENIDATE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
