Cevimeline Hydrochloride (Rising Pharmaceuticals, Inc.)
Welcome to the PulseAid listing for the Cevimeline Hydrochloride drug offered from Rising Pharmaceuticals, Inc.. This Cholinergic Muscarinic Agonists [MoA],Cholinergic Receptor Agonist [EPC] 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: | Rising Pharmaceuticals, Inc. |
| NON-PROPRIETARY NAME: | Cevimeline Hydrochloride |
| SUBSTANCE NAME: | CEVIMELINE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Cholinergic Muscarinic Agonists [MoA],Cholinergic Receptor Agonist [EPC] |
| ROUTE: | ORAL |
| DOSAGE FORM: | CAPSULE |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2014-06-17 |
| END MARKETING DATE: | 0000-00-00 |
Cevimeline Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Cevimeline Hydrochloride from Rising Pharmaceuticals, Inc. |
| LABELER NAME: | Rising Pharmaceuticals, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 30(mg/1) |
| START MARKETING DATE: | 2014-06-17 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 16571-657_5ad415e6-8a59-4ac6-aaa5-b095de6777b8 |
| PRODUCT NDC: | 16571-657 |
| APPLICATION NUMBER: | ANDA203775 |
Other CEVIMELINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
