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: | CAPSULE, EXTENDED RELEASE |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2017-07-05 |
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: | 25(mg/1) |
START MARKETING DATE: | 2017-07-05 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0093-5045_bf59fedb-4d5c-41d4-b652-f55e813f5c27 |
PRODUCT NDC: | 0093-5045 |
APPLICATION NUMBER: | ANDA202731 |
Other DEXMETHYLPHENIDATE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: