Amiloride Hydrochloride (Par Pharmaceutical Inc.)
Welcome to the PulseAid listing for the Amiloride Hydrochloride drug offered from Par Pharmaceutical 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: | Par Pharmaceutical Inc. |
| NON-PROPRIETARY NAME: | Amiloride Hydrochloride |
| SUBSTANCE NAME: | AMILORIDE HYDROCHLORIDE ANHYDROUS |
| 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: | 1986-01-22 |
| END MARKETING DATE: | 0000-00-00 |
Amiloride Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Amiloride Hydrochloride from Par Pharmaceutical Inc. |
| LABELER NAME: | Par Pharmaceutical Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 5(mg/1) |
| START MARKETING DATE: | 1986-01-22 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 49884-117_08c10863-8287-43be-9775-cf9f2a7a3b17 |
| PRODUCT NDC: | 49884-117 |
| APPLICATION NUMBER: | ANDA070346 |
Other AMILORIDE HYDROCHLORIDE ANHYDROUS Pharmaceutical Manufacturers / Labelers:
