Amiloride Hydrochloride and Hydrochlorothiazide (Teva Pharmaceuticals USA, Inc.)
Welcome to the PulseAid listing for the Amiloride Hydrochloride and Hydrochlorothiazide drug offered from Teva Pharmaceuticals USA, Inc.. This Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] 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: | Teva Pharmaceuticals USA, Inc. |
| NON-PROPRIETARY NAME: | Amiloride Hydrochloride and Hydrochlorothiazide |
| SUBSTANCE NAME: | AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 1989-12-01 |
| END MARKETING DATE: | 0000-00-00 |
Amiloride Hydrochloride and Hydrochlorothiazide HUMAN PRESCRIPTION DRUG Details:
| Item Description | Amiloride Hydrochloride and Hydrochlorothiazide from Teva Pharmaceuticals USA, Inc. |
| LABELER NAME: | Teva Pharmaceuticals USA, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 5; 50(mg/1; mg/1) |
| START MARKETING DATE: | 1989-12-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0555-0483_8dc14105-b775-4486-bf83-c7c1b5d40f17 |
| PRODUCT NDC: | 0555-0483 |
| APPLICATION NUMBER: | ANDA071111 |
Other AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE Pharmaceutical Manufacturers / Labelers:
