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Triamterene and Hydrochlorothiazide - 53808-0804-1 - (TRIAMTERENE AND HYDROCHLOROTHIAZIDE)

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Drug Information of Triamterene and Hydrochlorothiazide

Product NDC: 53808-0804
Proprietary Name: Triamterene and Hydrochlorothiazide
Non Proprietary Name: TRIAMTERENE AND HYDROCHLOROTHIAZIDE
Active Ingredient(s): 50; 75    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: 53808-0804
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071851
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Triamterene and Hydrochlorothiazide

Package NDC: 53808-0804-1
Package Description: 30 TABLET in 1 BLISTER PACK (53808-0804-1)

NDC Information of Triamterene and Hydrochlorothiazide

NDC Code 53808-0804-1
Proprietary Name Triamterene and Hydrochlorothiazide
Package Description 30 TABLET in 1 BLISTER PACK (53808-0804-1)
Product NDC 53808-0804
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TRIAMTERENE AND HYDROCHLOROTHIAZIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
Substance Name HYDROCHLOROTHIAZIDE; TRIAMTERENE
Strength Number 50; 75
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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