Hydrochlorothiazide

Product NDC
71335-1350
11-digit product format
713351350
Labeler code
71335
Product ID
71335-1350_4a8910de-61c1-4a1d-952f-e35268f493e2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hydrochlorothiazide
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA083177
Marketing category
ANDA
Marketing start
1973-01-12
Marketing end
0000-00-00
Substance
HYDROCHLOROTHIAZIDE
Active strength
25 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

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1350-071335135000120 TABLET in 1 BOTTLE (71335-1350-0) 120 tablet2022-06-290000-00-00NoNoCurrent
71335-1350-171335135001100 TABLET in 1 BOTTLE (71335-1350-1) 100 tablet2021-12-280000-00-00NoNoCurrent
71335-1350-27133513500230 TABLET in 1 BOTTLE (71335-1350-2) 30 tablet2022-06-290000-00-00NoNoCurrent
71335-1350-3713351350037 TABLET in 1 BOTTLE (71335-1350-3) 7 tablet2022-06-290000-00-00NoNoCurrent
71335-1350-47133513500414 TABLET in 1 BOTTLE (71335-1350-4) 14 tablet2022-06-290000-00-00NoNoCurrent
71335-1350-57133513500560 TABLET in 1 BOTTLE (71335-1350-5) 60 tablet2022-06-290000-00-00NoNoCurrent
71335-1350-6713351350062 TABLET in 1 BOTTLE (71335-1350-6) 2 tablet1973-01-120000-00-00NoNoCurrent
71335-1350-77133513500790 TABLET in 1 BOTTLE (71335-1350-7) 90 tablet1973-01-120000-00-00NoNoCurrent
71335-1350-8713351350084 TABLET in 1 BOTTLE (71335-1350-8) 4 tablet1973-01-120000-00-00NoNoCurrent
71335-1350-9713351350098 TABLET in 1 BOTTLE (71335-1350-9) 8 tablet1973-01-120000-00-00NoNoCurrent