HYDROCHLOROTHIAZIDE

Product NDC
71610-488
11-digit product format
716100488
Labeler code
71610
Product ID
71610-488_2b23f47e-94fc-4aa3-9545-aaa81fdd1400
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
HYDROCHLOROTHIAZIDE
Dosage form
TABLET
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
ANDA040702
Marketing category
ANDA
Marketing start
2007-03-16
Substance
HYDROCHLOROTHIAZIDE
Active strength
25 mg/1
Pharmacologic classes
Increased Diuresis [PE], 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

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71610-488-157161004881515 TABLET in 1 BOTTLE, PLASTIC (71610-488-15) 15 tablet2020-11-10NoNoHistorical
71610-488-307161004883030 TABLET in 1 BOTTLE, PLASTIC (71610-488-30) 30 tablet2020-11-10NoNoHistorical
71610-488-457161004884545 TABLET in 1 BOTTLE, PLASTIC (71610-488-45) 45 tablet2020-11-10NoNoHistorical
71610-488-537161004885360 TABLET in 1 BOTTLE, PLASTIC (71610-488-53) 60 tablet2020-11-10NoNoHistorical
71610-488-607161004886090 TABLET in 1 BOTTLE, PLASTIC (71610-488-60) 90 tablet2020-11-10NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
HYDROCHLOROTHIAZIDE TABLETS, USP Rx onlyAphena Pharma Solutions - Tennessee, LLC2020-12-14HUMAN PRESCRIPTION DRUG LABEL1