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Triamterene and Hydrochlorothiazide - 0781-2074-10 - (Triamterene and Hydrochlorothiazide)

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Drug Information of Triamterene and Hydrochlorothiazide

Product NDC: 0781-2074
Proprietary Name: Triamterene and Hydrochlorothiazide
Non Proprietary Name: Triamterene and Hydrochlorothiazide
Active Ingredient(s): 25; 37.5    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: 0781-2074
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074821
Marketing Category: ANDA
Start Marketing Date: 19970605

Package Information of Triamterene and Hydrochlorothiazide

Package NDC: 0781-2074-10
Package Description: 1000 CAPSULE in 1 BOTTLE (0781-2074-10)

NDC Information of Triamterene and Hydrochlorothiazide

NDC Code 0781-2074-10
Proprietary Name Triamterene and Hydrochlorothiazide
Package Description 1000 CAPSULE in 1 BOTTLE (0781-2074-10)
Product NDC 0781-2074
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Triamterene and Hydrochlorothiazide
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19970605
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name HYDROCHLOROTHIAZIDE; TRIAMTERENE
Strength Number 25; 37.5
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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