Olmesartan Medoxomil and Hydrochlorothiazide (Alembic Pharmaceuticals Inc.)
Welcome to the PulseAid listing for the Olmesartan Medoxomil and Hydrochlorothiazide drug offered from Alembic Pharmaceuticals 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: | Alembic Pharmaceuticals Inc. |
NON-PROPRIETARY NAME: | Olmesartan Medoxomil and 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 |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2017-04-24 |
END MARKETING DATE: | 0000-00-00 |
Olmesartan Medoxomil and Hydrochlorothiazide HUMAN PRESCRIPTION DRUG Details:
Item Description | Olmesartan Medoxomil and Hydrochlorothiazide from Alembic Pharmaceuticals Inc. |
LABELER NAME: | Alembic Pharmaceuticals Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 20; 12.5(mg/1; mg/1) |
START MARKETING DATE: | 2017-04-24 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 62332-149_af2556be-98d8-4659-ada4-143caa512fd9 |
PRODUCT NDC: | 62332-149 |
APPLICATION NUMBER: | ANDA204233 |
Other OLMESARTAN MEDOXOMIL; HYDROCHLOROTHIAZIDE Pharmaceutical Manufacturers / Labelers: