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Triamterene hydrochlorothiazide - 0781-1008-05 - (Triamterene and hydrochlorothiazide)

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Drug Information of Triamterene hydrochlorothiazide

Product NDC: 0781-1008
Proprietary Name: Triamterene hydrochlorothiazide
Non Proprietary Name: Triamterene and hydrochlorothiazide
Active Ingredient(s): 50; 75    mg/1; mg/1 & nbsp;   Triamterene and hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Triamterene hydrochlorothiazide

Product NDC: 0781-1008
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072011
Marketing Category: ANDA
Start Marketing Date: 19880617

Package Information of Triamterene hydrochlorothiazide

Package NDC: 0781-1008-05
Package Description: 500 TABLET in 1 BOTTLE (0781-1008-05)

NDC Information of Triamterene hydrochlorothiazide

NDC Code 0781-1008-05
Proprietary Name Triamterene hydrochlorothiazide
Package Description 500 TABLET in 1 BOTTLE (0781-1008-05)
Product NDC 0781-1008
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Triamterene and hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19880617
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name HYDROCHLOROTHIAZIDE; TRIAMTERENE
Strength Number 50; 75
Strength Unit mg/1; mg/1
Pharmaceutical Classes Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Triamterene hydrochlorothiazide


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