Bisoprolol Fumarate and Hydrochlorothiazide (Eon Labs, Inc.)
Welcome to the PulseAid listing for the Bisoprolol Fumarate and Hydrochlorothiazide drug offered from Eon Labs, Inc.. This Adrenergic beta-Antagonists [MoA],beta-Adrenergic 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: | Eon Labs, Inc. |
| NON-PROPRIETARY NAME: | Bisoprolol Fumarate and Hydrochlorothiazide |
| SUBSTANCE NAME: | BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, COATED |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2000-09-25 |
| END MARKETING DATE: | 0000-00-00 |
Bisoprolol Fumarate and Hydrochlorothiazide HUMAN PRESCRIPTION DRUG Details:
| Item Description | Bisoprolol Fumarate and Hydrochlorothiazide from Eon Labs, Inc. |
| LABELER NAME: | Eon Labs, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 2.5; 6.25(mg/1; mg/1) |
| START MARKETING DATE: | 2000-09-25 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0185-0701_9e881d2a-7d0f-48ec-8d35-921130c8a604 |
| PRODUCT NDC: | 0185-0701 |
| APPLICATION NUMBER: | ANDA075579 |
Other BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE Pharmaceutical Manufacturers / Labelers:
