NDC 0172-2089

Hydrochlorothiazide

Hydrochlorothiazide

Hydrochlorothiazide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Teva Pharmaceuticals Usa, Inc.. The primary component is Hydrochlorothiazide.

Product ID0172-2089_1b6494dd-00e4-435e-a321-0a2f1706ccf4
NDC0172-2089
Product TypeHuman Prescription Drug
Proprietary NameHydrochlorothiazide
Generic NameHydrochlorothiazide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1980-01-07
Marketing CategoryANDA / ANDA
Application NumberANDA083177
Labeler NameTeva Pharmaceuticals USA, Inc.
Substance NameHYDROCHLOROTHIAZIDE
Active Ingredient Strength50 mg/1
Pharm ClassesIncreased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 0172-2089-60

100 TABLET in 1 BOTTLE (0172-2089-60)
Marketing Start Date1980-01-08
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0172-2089-31 [00172208931]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA083177
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1980-01-07
Marketing End Date2010-01-12

NDC 0172-2089-85 [00172208985]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA083177
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1982-06-29
Marketing End Date2015-03-31

NDC 0172-2089-00 [00172208900]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA083177
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1980-01-07
Marketing End Date2014-03-12

NDC 0172-2089-95 [00172208995]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA083177
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1980-01-07
Marketing End Date2010-01-12

NDC 0172-2089-60 [00172208960]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA083177
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1980-01-08

NDC 0172-2089-10 [00172208910]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA083177
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1980-01-07
Marketing End Date2014-03-12

NDC 0172-2089-80 [00172208980]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA083177
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1980-01-07

NDC 0172-2089-71 [00172208971]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA083177
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1980-01-07
Marketing End Date2010-01-12

Drug Details

Active Ingredients

IngredientStrength
HYDROCHLOROTHIAZIDE50 mg/1

OpenFDA Data

SPL SET ID:e2270db4-2930-4ec5-ac96-2b4542aed367
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310798
  • 197770

    • 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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