Dexmethylphenidate Hydrochloride (Sandoz Inc)
Welcome to the PulseAid listing for the Dexmethylphenidate Hydrochloride drug offered from Sandoz 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: | Sandoz 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: | NDA AUTHORIZED GENERIC |
| START MARKETING DATE: | 2015-04-27 |
| END MARKETING DATE: | 0000-00-00 |
Dexmethylphenidate Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Dexmethylphenidate Hydrochloride from Sandoz Inc |
| LABELER NAME: | Sandoz Inc |
| DEA SCHEDULE: | CII
|
| ACTIVE STRENGTH: | 2.5(mg/1) |
| START MARKETING DATE: | 2015-04-27 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0781-5676_5dce18f6-7f59-4726-9971-d3fa6e459959 |
| PRODUCT NDC: | 0781-5676 |
| APPLICATION NUMBER: | NDA021278 |
Other DEXMETHYLPHENIDATE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
