bisoprolol fumarate and hydrochlorothiazide (NuCare Pharmaceuticals, Inc.)
Welcome to the PulseAid listing for the bisoprolol fumarate and hydrochlorothiazide drug offered from NuCare Pharmaceuticals, Inc.. This Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Adrenergic beta-Antagonists [MoA],beta-Adrenergic 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: | NuCare Pharmaceuticals, Inc. |
NON-PROPRIETARY NAME: | bisoprolol fumarate and hydrochlorothiazide |
SUBSTANCE NAME: | HYDROCHLOROTHIAZIDE; BISOPROLOL FUMARATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2010-10-12 |
END MARKETING DATE: | 0000-00-00 |
bisoprolol fumarate and hydrochlorothiazide HUMAN PRESCRIPTION DRUG Details:
Item Description | bisoprolol fumarate and hydrochlorothiazide from NuCare Pharmaceuticals, Inc. |
LABELER NAME: | NuCare Pharmaceuticals, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 6.25; 10(mg/1; mg/1) |
START MARKETING DATE: | 2010-10-12 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 68071-2131_540ee876-78f7-1792-e054-00144ff88e88 |
PRODUCT NDC: | 68071-2131 |
APPLICATION NUMBER: | ANDA079106 |
Other HYDROCHLOROTHIAZIDE; BISOPROLOL FUMARATE Pharmaceutical Manufacturers / Labelers: