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Triamterene hydrochlorothiazide - 54868-2679-5 - (Triamterene and hydrochlorothiazide)

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Drug Information of Triamterene hydrochlorothiazide

Product NDC: 54868-2679
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: 54868-2679
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073281
Marketing Category: ANDA
Start Marketing Date: 19990219

Package Information of Triamterene hydrochlorothiazide

Package NDC: 54868-2679-5
Package Description: 90 TABLET in 1 BOTTLE (54868-2679-5)

NDC Information of Triamterene hydrochlorothiazide

NDC Code 54868-2679-5
Proprietary Name Triamterene hydrochlorothiazide
Package Description 90 TABLET in 1 BOTTLE (54868-2679-5)
Product NDC 54868-2679
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Triamterene and hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19990219
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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 hydrochlorothiazide


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