Dexmethylphenidate Hydrochloride Extended-Release (American Health Packaging)
Welcome to the PulseAid listing for the Dexmethylphenidate Hydrochloride Extended-Release drug offered from American Health Packaging. 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: | American Health Packaging |
| 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: | 2015-03-31 |
| END MARKETING DATE: | 2018-06-30 |
Dexmethylphenidate Hydrochloride Extended-Release HUMAN PRESCRIPTION DRUG Details:
| Item Description | Dexmethylphenidate Hydrochloride Extended-Release from American Health Packaging |
| LABELER NAME: | American Health Packaging |
| DEA SCHEDULE: | CII
|
| ACTIVE STRENGTH: | 30(mg/1) |
| START MARKETING DATE: | 2015-03-31 |
| END MARKETING DATE: | 2018-06-30 |
| PRODUCT ID: | 68084-933_55d97d0a-5f1d-196c-e054-00144ff88e88 |
| PRODUCT NDC: | 68084-933 |
| APPLICATION NUMBER: | ANDA078992 |
Other DEXMETHYLPHENIDATE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
