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Triamterene hydrochlorothiazide - 63629-2647-2 - (Triamterene and hydrochlorothiazide)

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Drug Information of Triamterene hydrochlorothiazide

Product NDC: 63629-2647
Proprietary Name: Triamterene 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): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Triamterene hydrochlorothiazide

Product NDC: 63629-2647
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073281
Marketing Category: ANDA
Start Marketing Date: 19920430

Package Information of Triamterene hydrochlorothiazide

Package NDC: 63629-2647-2
Package Description: 90 TABLET in 1 BOTTLE (63629-2647-2)

NDC Information of Triamterene hydrochlorothiazide

NDC Code 63629-2647-2
Proprietary Name Triamterene hydrochlorothiazide
Package Description 90 TABLET in 1 BOTTLE (63629-2647-2)
Product NDC 63629-2647
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Triamterene and hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19920430
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
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 hydrochlorothiazide


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