NDC 71335-0652

Hydrochlorothiazide

Hydrochlorothiazide

Hydrochlorothiazide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Hydrochlorothiazide.

Product ID71335-0652_73bc116a-2964-4acc-9ef0-0a3f66268913
NDC71335-0652
Product TypeHuman Prescription Drug
Proprietary NameHydrochlorothiazide
Generic NameHydrochlorothiazide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2008-08-15
Marketing CategoryANDA / ANDA
Application NumberANDA040907
Labeler NameBryant Ranch Prepack
Substance NameHYDROCHLOROTHIAZIDE
Active Ingredient Strength25 mg/1
Pharm ClassesIncreased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 71335-0652-0

8 TABLET in 1 BOTTLE (71335-0652-0)
Marketing Start Date2021-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0652-1 [71335065201]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040907
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-11-03

NDC 71335-0652-7 [71335065207]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040907
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-11-03

NDC 71335-0652-9 [71335065209]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040907
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-11-03

NDC 71335-0652-5 [71335065205]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040907
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-11-03

NDC 71335-0652-2 [71335065202]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040907
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-11-03

NDC 71335-0652-8 [71335065208]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040907
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-11-03

NDC 71335-0652-4 [71335065204]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040907
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-11-03

NDC 71335-0652-6 [71335065206]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040907
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-11-03

NDC 71335-0652-3 [71335065203]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040907
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-11-03

NDC 71335-0652-0 [71335065200]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040907
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-11-03

Drug Details

Active Ingredients

IngredientStrength
HYDROCHLOROTHIAZIDE25 mg/1

OpenFDA Data

SPL SET ID:73bc116a-2964-4acc-9ef0-0a3f66268913
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310798

    • Pharmacological Class

    • Increased Diuresis [PE]
    • Thiazide Diuretic [EPC]
    • Thiazides [CS]

    NDC Crossover Matching brand name "Hydrochlorothiazide" or generic name "Hydrochlorothiazide"

    NDCBrand NameGeneric Name
    0143-1256HydrochlorothiazideHydrochlorothiazide
    0143-1257HydrochlorothiazideHydrochlorothiazide
    0143-3125HydrochlorothiazideHydrochlorothiazide
    0172-2083HydrochlorothiazideHydrochlorothiazide
    0172-2089HydrochlorothiazideHydrochlorothiazide
    0179-0065HydrochlorothiazideHydrochlorothiazide
    0228-2820HydrochlorothiazideHydrochlorothiazide
    0378-0810Hydrochlorothiazidehydrochlorothiazide
    0440-1595HydrochlorothiazideHydrochlorothiazide
    0440-7595HydrochlorothiazideHydrochlorothiazide
    0527-1413HydrochlorothiazideHydrochlorothiazide
    0527-1414HydrochlorothiazideHydrochlorothiazide
    0527-1635HydrochlorothiazideHydrochlorothiazide
    0591-0347HydrochlorothiazideHydrochlorothiazide
    0615-1358HydrochlorothiazideHydrochlorothiazide
    0615-1561HydrochlorothiazideHydrochlorothiazide
    0615-1562HydrochlorothiazideHydrochlorothiazide
    0615-7974HydrochlorothiazideHydrochlorothiazide
    0615-8036Hydrochlorothiazidehydrochlorothiazide
    0615-8149HydrochlorothiazideHydrochlorothiazide
    0615-8344HydrochlorothiazideHydrochlorothiazide
    10544-028HydrochlorothiazideHydrochlorothiazide
    10544-047HydrochlorothiazideHydrochlorothiazide
    10544-105HydrochlorothiazideHydrochlorothiazide
    10544-136HydrochlorothiazideHydrochlorothiazide
    10544-197HydrochlorothiazideHydrochlorothiazide
    10544-198HydrochlorothiazideHydrochlorothiazide
    68071-1255hydrochlorothiazidehydrochlorothiazide
    68071-1736HYDROCHLOROTHIAZIDEHYDROCHLOROTHIAZIDE
    68071-3238HydrochlorothiazideHydrochlorothiazide
    68071-3215HYDROCHLOROTHIAZIDEHYDROCHLOROTHIAZIDE
    68071-3323HydrochlorothiazideHydrochlorothiazide
    68071-4176HydrochlorothiazideHydrochlorothiazide
    68071-4361HydrochlorothiazideHydrochlorothiazide
    68071-4438HydrochlorothiazideHydrochlorothiazide
    68071-4819HydrochlorothiazideHydrochlorothiazide
    68071-4807HydrochlorothiazideHydrochlorothiazide
    68071-4758HydrochlorothiazideHydrochlorothiazide
    68151-2757HydrochlorothiazideHydrochlorothiazide
    68151-2781HydrochlorothiazideHydrochlorothiazide
    68645-340HydrochlorothiazideHydrochlorothiazide
    68645-341HydrochlorothiazideHydrochlorothiazide
    68645-511HydrochlorothiazideHydrochlorothiazide
    68645-510HydrochlorothiazideHydrochlorothiazide
    68788-6844HydrochlorothiazideHydrochlorothiazide
    68788-8928HydrochlorothiazideHydrochlorothiazide
    68788-7400HydrochlorothiazideHydrochlorothiazide
    68788-9401HydrochlorothiazideHydrochlorothiazide
    68788-9920HydrochlorothiazideHydrochlorothiazide
    68788-9919HydrochlorothiazideHydrochlorothiazide
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