DYAZIDE (GlaxoSmithKline LLC)
Welcome to the PulseAid listing for the DYAZIDE drug offered from GlaxoSmithKline LLC. This Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [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: | GlaxoSmithKline LLC |
NON-PROPRIETARY NAME: | hydrochlorothiazide and triamterene |
SUBSTANCE NAME: | HYDROCHLOROTHIAZIDE; TRIAMTERENE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC] |
ROUTE: | ORAL |
DOSAGE FORM: | CAPSULE |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 1994-03-30 |
END MARKETING DATE: | 0000-00-00 |
DYAZIDE HUMAN PRESCRIPTION DRUG Details:
Item Description | DYAZIDE from GlaxoSmithKline LLC |
LABELER NAME: | GlaxoSmithKline LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 25; 37.5(mg/1; mg/1) |
START MARKETING DATE: | 1994-03-30 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0007-3650_25b16f40-16dd-429b-ba22-5878756b0fe1 |
PRODUCT NDC: | 0007-3650 |
APPLICATION NUMBER: | NDA016042 |
Other HYDROCHLOROTHIAZIDE; TRIAMTERENE Pharmaceutical Manufacturers / Labelers: