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: |
|
| 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:
