amiloride hydrochloride (Zydus Pharmaceuticals (USA) Inc.)
Welcome to the PulseAid listing for the amiloride hydrochloride drug offered from Zydus Pharmaceuticals (USA) Inc.. This Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [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: | Zydus Pharmaceuticals (USA) Inc. |
| NON-PROPRIETARY NAME: | amiloride hydrochloride |
| SUBSTANCE NAME: | AMILORIDE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2015-09-14 |
| END MARKETING DATE: | 0000-00-00 |
amiloride hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | amiloride hydrochloride from Zydus Pharmaceuticals (USA) Inc. |
| LABELER NAME: | Zydus Pharmaceuticals (USA) Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 5(mg/1) |
| START MARKETING DATE: | 2015-09-14 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 68382-671_afc33e3e-2491-4721-8ea3-09e906cc67f1 |
| PRODUCT NDC: | 68382-671 |
| APPLICATION NUMBER: | ANDA204180 |
Other AMILORIDE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
