Home > National Drug Code (NDC) > Triamterene and Hydrochlorothiazide

Triamterene and Hydrochlorothiazide - 68788-9792-3 - (Triamterene and Hydrochlorothiazide)

Alphabetical Index


Drug Information of Triamterene and Hydrochlorothiazide

Product NDC: 68788-9792
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: 68788-9792
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071851
Marketing Category: ANDA
Start Marketing Date: 20120430

Package Information of Triamterene and Hydrochlorothiazide

Package NDC: 68788-9792-3
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (68788-9792-3)

NDC Information of Triamterene and Hydrochlorothiazide

NDC Code 68788-9792-3
Proprietary Name Triamterene and Hydrochlorothiazide
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (68788-9792-3)
Product NDC 68788-9792
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Triamterene and Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120430
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
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


General Information