Metoprolol Tartrate and Hydrochlorothiazide50 mg-25 mg (NorthStar RxLLC)
Welcome to the PulseAid listing for the Metoprolol Tartrate and Hydrochlorothiazide drug offered from NorthStar RxLLC. 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: | NorthStar RxLLC |
NON-PROPRIETARY NAME: | Metoprolol Tartrate and Hydrochlorothiazide |
SUBSTANCE NAME: | METOPROLOL TARTRATE; HYDROCHLOROTHIAZIDE |
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: | 2013-09-17 |
END MARKETING DATE: | 0000-00-00 |
Metoprolol Tartrate and Hydrochlorothiazide 50 mg-25 mg HUMAN PRESCRIPTION DRUG Details:
Item Description | Metoprolol Tartrate and Hydrochlorothiazide 50 mg-25 mg from NorthStar RxLLC |
LABELER NAME: | NorthStar RxLLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 50; 25(mg/1; mg/1) |
START MARKETING DATE: | 2013-09-17 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 16714-417_ff0239c9-dacb-4f86-8ad8-7f1a01432227 |
PRODUCT NDC: | 16714-417 |
APPLICATION NUMBER: | ANDA202870 |
Other METOPROLOL TARTRATE; HYDROCHLOROTHIAZIDE Pharmaceutical Manufacturers / Labelers: