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Triamterene and Hydrochlorothiazide - 16590-338-30 - (Triamterene and Hydrochlorothiazide)

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Drug Information of Triamterene and Hydrochlorothiazide

Product NDC: 16590-338
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: 16590-338
Labeler Name: STAT Rx USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073449
Marketing Category: ANDA
Start Marketing Date: 19930923

Package Information of Triamterene and Hydrochlorothiazide

Package NDC: 16590-338-30
Package Description: 30 TABLET in 1 BOTTLE (16590-338-30)

NDC Information of Triamterene and Hydrochlorothiazide

NDC Code 16590-338-30
Proprietary Name Triamterene and Hydrochlorothiazide
Package Description 30 TABLET in 1 BOTTLE (16590-338-30)
Product NDC 16590-338
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Triamterene and Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19930923
Marketing Category Name ANDA
Labeler Name STAT Rx USA LLC
Substance Name HYDROCHLOROTHIAZIDE; TRIAMTERENE
Strength Number 25; 37.5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC]

Complete Information of Triamterene and Hydrochlorothiazide


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