Mecamylamine Hydrochloride (Nexgen Pharma, Inc.)
Welcome to the PulseAid listing for the Mecamylamine Hydrochloride drug offered from Nexgen Pharma, Inc.. This Autonomic Ganglionic Blocker [EPC],Decreased Autonomic Ganglionic Activity [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: | Nexgen Pharma, Inc. |
| NON-PROPRIETARY NAME: | Mecamylamine Hydrochloride |
| SUBSTANCE NAME: | MECAMYLAMINE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Autonomic Ganglionic Blocker [EPC],Decreased Autonomic Ganglionic Activity [PE] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2013-03-19 |
| END MARKETING DATE: | 0000-00-00 |
Mecamylamine Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Mecamylamine Hydrochloride from Nexgen Pharma, Inc. |
| LABELER NAME: | Nexgen Pharma, Inc. |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | 2.5(mg/1) |
| START MARKETING DATE: | 2013-03-19 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0722-7183_b87994ee-26a5-4d00-99e7-796bc17961f1 |
| PRODUCT NDC: | 0722-7183 |
| APPLICATION NUMBER: | ANDA204054 |
Other MECAMYLAMINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
