HYDROCHLOROTHIAZIDE

Product NDC
71335-1716
11-digit product format
713351716
Labeler code
71335
Product ID
71335-1716_0312f173-ee68-47fe-bca1-67f0498d681b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
hydrochlorothiazide
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA085182
Marketing category
ANDA
Marketing start
2015-01-15
Marketing end
0000-00-00
Substance
HYDROCHLOROTHIAZIDE
Active strength
50 mg/1
Pharmacologic classes
Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
0J48LPH2THHYDROCHLOROTHIAZIDE58-93-5HYDROCHLOROTHIAZIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1716-07133517160045 TABLET in 1 BOTTLE (71335-1716-0) 45 tablet2022-01-280000-00-00NoNoCurrent
71335-1716-17133517160130 TABLET in 1 BOTTLE (71335-1716-1) 30 tablet2020-10-260000-00-00NoNoCurrent
71335-1716-27133517160260 TABLET in 1 BOTTLE (71335-1716-2) 60 tablet2022-01-280000-00-00NoNoCurrent
71335-1716-37133517160390 TABLET in 1 BOTTLE (71335-1716-3) 90 tablet2020-12-070000-00-00NoNoCurrent
71335-1716-47133517160428 TABLET in 1 BOTTLE (71335-1716-4) 28 tablet2022-01-280000-00-00NoNoCurrent
71335-1716-57133517160556 TABLET in 1 BOTTLE (71335-1716-5) 56 tablet2022-01-280000-00-00NoNoCurrent
71335-1716-671335171606100 TABLET in 1 BOTTLE (71335-1716-6) 100 tablet2020-10-260000-00-00NoNoCurrent
71335-1716-7713351716077 TABLET in 1 BOTTLE (71335-1716-7) 7 tablet2020-10-260000-00-00NoNoCurrent
71335-1716-87133517160814 TABLET in 1 BOTTLE (71335-1716-8) 14 tablet2020-10-260000-00-00NoNoCurrent
71335-1716-971335171609120 TABLET in 1 BOTTLE (71335-1716-9) 120 tablet2020-10-260000-00-00NoNoCurrent