Triamterene and Hydrochlorothiazide

Product NDC
63629-2585
11-digit product format
636292585
Labeler code
63629
Product ID
63629-2585_b5846d98-0f70-4df4-8f9a-13780b09f96a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Triamterene and Hydrochlorothiazide
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA071851
Marketing category
ANDA
Marketing start
1993-09-23
Substance
HYDROCHLOROTHIAZIDE; TRIAMTERENE
Active strength
50; 75 mg/1; mg/1
Pharmacologic classes
Decreased Renal K+ Excretion [PE], Increased Diuresis [PE], Increased Diuresis [PE], Potassium-sparing Diuretic [EPC], Thiazide Diuretic [EPC], Thiazides [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
0J48LPH2THHYDROCHLOROTHIAZIDE58-93-5HYDROCHLOROTHIAZIDE
WS821Z52LQTRIAMTERENE396-01-0TRIAMTERENE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
63629-2585-16362925850130 TABLET in 1 BOTTLE (63629-2585-1) 30 tablet2005-01-07NoNoHistorical
63629-2585-26362925850215 TABLET in 1 BOTTLE (63629-2585-2) 15 tablet2010-09-23NoNoHistorical
63629-2585-36362925850390 TABLET in 1 BOTTLE (63629-2585-3) 90 tablet2015-07-31NoNoHistorical
63629-2585-463629258504100 TABLET in 1 BOTTLE (63629-2585-4) 100 tablet2021-12-22NoNoHistorical
63629-2585-5636292585057 TABLET in 1 BOTTLE (63629-2585-5) 7 tablet2019-09-25NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Triamterene and Hydrochlorothiazide Tablets, USP Revised: November 2020 Rx onlyBryant Ranch Prepack2024-05-22HUMAN PRESCRIPTION DRUG LABEL12