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: