Losartan Potassium and Hydrochlorothiazide (REMEDYREPACK INC.)
Welcome to the PulseAid listing for the Losartan Potassium and Hydrochlorothiazide drug offered from REMEDYREPACK INC.. This Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [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: | REMEDYREPACK INC. |
NON-PROPRIETARY NAME: | Losartan Potassium and Hydrochlorothiazide |
SUBSTANCE NAME: | HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2013-01-24 |
END MARKETING DATE: | 0000-00-00 |
Losartan Potassium and Hydrochlorothiazide HUMAN PRESCRIPTION DRUG Details:
Item Description | Losartan Potassium and Hydrochlorothiazide from REMEDYREPACK INC. |
LABELER NAME: | REMEDYREPACK INC. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 12.5; 100(mg/1; mg/1) |
START MARKETING DATE: | 2013-01-24 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 52125-452_476c8d8c-a551-5515-e054-00144ff88e88 |
PRODUCT NDC: | 52125-452 |
APPLICATION NUMBER: | ANDA090528 |
Other HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM Pharmaceutical Manufacturers / Labelers: