Olmesartan Medoxomil and Hydrochlorothiazide (Sun Pharmaceutical Industries, Inc.)
Welcome to the PulseAid listing for the Olmesartan Medoxomil and Hydrochlorothiazide drug offered from Sun Pharmaceutical Industries, Inc.. This Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [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: | Sun Pharmaceutical Industries, Inc. |
NON-PROPRIETARY NAME: | olmesartan medoxomil-hydrochlorothiazide |
SUBSTANCE NAME: | OLMESARTAN MEDOXOMIL; HYDROCHLOROTHIAZIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, FILM COATED |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2016-10-26 |
END MARKETING DATE: | 0000-00-00 |
Olmesartan Medoxomil and Hydrochlorothiazide HUMAN PRESCRIPTION DRUG Details:
Item Description | Olmesartan Medoxomil and Hydrochlorothiazide from Sun Pharmaceutical Industries, Inc. |
LABELER NAME: | Sun Pharmaceutical Industries, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 20; 12.5(mg/1; mg/1) |
START MARKETING DATE: | 2016-10-26 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 57664-758_7853d97b-9011-4a03-8036-18fc9c220f5f |
PRODUCT NDC: | 57664-758 |
APPLICATION NUMBER: | NDA021532 |
Other OLMESARTAN MEDOXOMIL; HYDROCHLOROTHIAZIDE Pharmaceutical Manufacturers / Labelers: