Memantine Hydrochloride (Amneal Pharmaceuticals LLC)
Welcome to the PulseAid listing for the Memantine Hydrochloride drug offered from Amneal Pharmaceuticals LLC. This 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: | Amneal Pharmaceuticals LLC |
| NON-PROPRIETARY NAME: | Memantine Hydrochloride |
| SUBSTANCE NAME: | |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | |
| DOSAGE FORM: | KIT |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2014-04-30 |
| END MARKETING DATE: | 0000-00-00 |
Memantine Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Memantine Hydrochloride from Amneal Pharmaceuticals LLC |
| LABELER NAME: | Amneal Pharmaceuticals LLC |
| DEA SCHEDULE: | |
| ACTIVE STRENGTH: | () |
| START MARKETING DATE: | 2014-04-30 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 65162-707_8aa8da2b-d206-40d3-8e46-bb1dc14677cc |
| PRODUCT NDC: | 65162-707 |
| APPLICATION NUMBER: | ANDA205825 |