Losartan Potassium and Hydrochlorothiazide (Lupin Pharmaceuticals, Inc.)
Welcome to the PulseAid listing for the Losartan Potassium and Hydrochlorothiazide drug offered from Lupin Pharmaceuticals, 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: | Lupin Pharmaceuticals, 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: | 2010-10-06 |
END MARKETING DATE: | 0000-00-00 |
Losartan Potassium and Hydrochlorothiazide HUMAN PRESCRIPTION DRUG Details:
Item Description | Losartan Potassium and Hydrochlorothiazide from Lupin Pharmaceuticals, Inc. |
LABELER NAME: | Lupin Pharmaceuticals, Inc. |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 12.5; 50(mg/1; mg/1) |
START MARKETING DATE: | 2010-10-06 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 68180-215_2a7cd432-a523-4b53-9e1e-9808dbc4412f |
PRODUCT NDC: | 68180-215 |
APPLICATION NUMBER: | ANDA078245 |
Other HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM Pharmaceutical Manufacturers / Labelers: