Hydrochlorothiazide

Product NDC
71335-1481
11-digit product format
713351481
Labeler code
71335
Product ID
71335-1481_046b6751-595e-4fd5-96de-d5697238026f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hydrochlorothiazide
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA040412
Marketing category
ANDA
Marketing start
2002-03-29
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

Additional Listing Data#

Finished product
Yes
Brand name base
Hydrochlorothiazide
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
HYDROCHLOROTHIAZIDE25 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii0J48LPH2TH
Rxcui197770, 310798

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1481-071335148100120 TABLET in 1 BOTTLE (71335-1481-0) 120 tablet2002-03-290000-00-00NoNoCurrent
71335-1481-171335148101100 TABLET in 1 BOTTLE (71335-1481-1) 100 tablet2002-03-290000-00-00NoNoCurrent
71335-1481-27133514810230 TABLET in 1 BOTTLE (71335-1481-2) 30 tablet2002-03-290000-00-00NoNoCurrent
71335-1481-3713351481037 TABLET in 1 BOTTLE (71335-1481-3) 7 tablet2002-03-290000-00-00NoNoCurrent
71335-1481-47133514810414 TABLET in 1 BOTTLE (71335-1481-4) 14 tablet2002-03-290000-00-00NoNoCurrent
71335-1481-57133514810560 TABLET in 1 BOTTLE (71335-1481-5) 60 tablet2002-03-290000-00-00NoNoCurrent
71335-1481-6713351481062 TABLET in 1 BOTTLE (71335-1481-6) 2 tablet2002-03-290000-00-00NoNoCurrent
71335-1481-77133514810790 TABLET in 1 BOTTLE (71335-1481-7) 90 tablet2002-03-290000-00-00NoNoCurrent
71335-1481-8713351481084 TABLET in 1 BOTTLE (71335-1481-8) 4 tablet2002-03-290000-00-00NoNoCurrent
71335-1481-9713351481098 TABLET in 1 BOTTLE (71335-1481-9) 8 tablet2002-03-290000-00-00NoNoCurrent