Amiloride Hydrochloride and Hydrochlorothiazide (Mylan Pharmaceuticals Inc.)
Welcome to the PulseAid listing for the Amiloride Hydrochloride and Hydrochlorothiazide drug offered from Mylan Pharmaceuticals 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: | Mylan Pharmaceuticals 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: | 1991-10-31 |
END MARKETING DATE: | 0000-00-00 |
Amiloride Hydrochloride and Hydrochlorothiazide HUMAN PRESCRIPTION DRUG Details:
Item Description | Amiloride Hydrochloride and Hydrochlorothiazide from Mylan Pharmaceuticals Inc. |
LABELER NAME: | Mylan Pharmaceuticals Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 5; 50(mg/1; mg/1) |
START MARKETING DATE: | 1991-10-31 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0378-0577_bc568ed8-6312-4d66-9ea5-80ca9424343e |
PRODUCT NDC: | 0378-0577 |
APPLICATION NUMBER: | ANDA073209 |
Other AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE Pharmaceutical Manufacturers / Labelers: