NDC 53217-232

HYDROCHLOROTHIAZIDE

Hydrochlorothiazide

HYDROCHLOROTHIAZIDE is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Aidarex Pharmaceuticals Llc. The primary component is Hydrochlorothiazide.

Product ID53217-232_2867b2a2-bc97-42ef-b4a7-4c7afc448d67
NDC53217-232
Product TypeHuman Prescription Drug
Proprietary NameHYDROCHLOROTHIAZIDE
Generic NameHydrochlorothiazide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2007-03-01
Marketing CategoryANDA / ANDA
Application NumberANDA040702
Labeler NameAidarex Pharmaceuticals LLC
Substance NameHYDROCHLOROTHIAZIDE
Active Ingredient Strength25 mg/1
Pharm ClassesIncreased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 53217-232-90

90 TABLET in 1 BOTTLE (53217-232-90)
Marketing Start Date2007-03-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 53217-232-60 [53217023260]

HYDROCHLOROTHIAZIDE TABLET
Marketing CategoryANDA
Application NumberANDA040702
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-01
Inactivation Date2020-01-31

NDC 53217-232-90 [53217023290]

HYDROCHLOROTHIAZIDE TABLET
Marketing CategoryANDA
Application NumberANDA040702
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-01
Inactivation Date2020-01-31

NDC 53217-232-30 [53217023230]

HYDROCHLOROTHIAZIDE TABLET
Marketing CategoryANDA
Application NumberANDA040702
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-01
Inactivation Date2020-01-31

NDC 53217-232-00 [53217023200]

HYDROCHLOROTHIAZIDE TABLET
Marketing CategoryANDA
Application NumberANDA040702
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-01
Inactivation Date2020-01-31

NDC 53217-232-14 [53217023214]

HYDROCHLOROTHIAZIDE TABLET
Marketing CategoryANDA
Application NumberANDA040702
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
HYDROCHLOROTHIAZIDE25 mg/1

OpenFDA Data

SPL SET ID:034eb68d-6120-417e-9c6b-46f1314d0fd7
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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