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Triamterene and Hydrochlorothiazide - 60505-2656-5 - (Triamterene and Hydrochlorothiazide)

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Drug Information of Triamterene and Hydrochlorothiazide

Product NDC: 60505-2656
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): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Triamterene and Hydrochlorothiazide

Product NDC: 60505-2656
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071251
Marketing Category: ANDA
Start Marketing Date: 20090921

Package Information of Triamterene and Hydrochlorothiazide

Package NDC: 60505-2656-5
Package Description: 500 TABLET in 1 BOTTLE (60505-2656-5)

NDC Information of Triamterene and Hydrochlorothiazide

NDC Code 60505-2656-5
Proprietary Name Triamterene and Hydrochlorothiazide
Package Description 500 TABLET in 1 BOTTLE (60505-2656-5)
Product NDC 60505-2656
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Triamterene and Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090921
Marketing Category Name ANDA
Labeler Name Apotex Corp.
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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