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Triamterene and Hydrochlorothiazide - 0781-2715-13 - (Triamterene and Hydrochlorothiazide)

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Drug Information of Triamterene and Hydrochlorothiazide

Product NDC: 0781-2715
Proprietary Name: Triamterene and Hydrochlorothiazide
Non Proprietary Name: Triamterene and Hydrochlorothiazide
Active Ingredient(s): 25; 50    mg/1; mg/1 & nbsp;   Triamterene and Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Triamterene and Hydrochlorothiazide

Product NDC: 0781-2715
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073191
Marketing Category: ANDA
Start Marketing Date: 19910731

Package Information of Triamterene and Hydrochlorothiazide

Package NDC: 0781-2715-13
Package Description: 10 BLISTER PACK in 1 CARTON (0781-2715-13) > 10 CAPSULE in 1 BLISTER PACK

NDC Information of Triamterene and Hydrochlorothiazide

NDC Code 0781-2715-13
Proprietary Name Triamterene and Hydrochlorothiazide
Package Description 10 BLISTER PACK in 1 CARTON (0781-2715-13) > 10 CAPSULE in 1 BLISTER PACK
Product NDC 0781-2715
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Triamterene and Hydrochlorothiazide
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19910731
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name HYDROCHLOROTHIAZIDE; TRIAMTERENE
Strength Number 25; 50
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 and Hydrochlorothiazide


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