Propranolol Hydrochloride and Hydrochlorothiazide (Mylan Pharmaceuticals Inc.)
Welcome to the PulseAid listing for the Propranolol Hydrochloride and Hydrochlorothiazide drug offered from Mylan Pharmaceuticals 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: | Mylan Pharmaceuticals Inc. |
NON-PROPRIETARY NAME: | propranolol hydrochloride and hydrochlorothiazide |
SUBSTANCE NAME: | PROPRANOLOL HYDROCHLORIDE; 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 |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 1987-04-01 |
END MARKETING DATE: | 0000-00-00 |
Propranolol Hydrochloride and Hydrochlorothiazide HUMAN PRESCRIPTION DRUG Details:
Item Description | Propranolol Hydrochloride and Hydrochlorothiazide from Mylan Pharmaceuticals Inc. |
LABELER NAME: | Mylan Pharmaceuticals Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 80; 25(mg/1; mg/1) |
START MARKETING DATE: | 1987-04-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0378-0347_fa0d6a3f-e297-45e5-ad1f-f08787db0227 |
PRODUCT NDC: | 0378-0347 |
APPLICATION NUMBER: | ANDA070947 |
Other PROPRANOLOL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE Pharmaceutical Manufacturers / Labelers: