NDC 63629-6377

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 ID63629-6377_e0ab2a3a-f05f-4071-a7c5-8ddf1ba09d7c
NDC63629-6377
Product TypeHuman Prescription Drug
Proprietary NameHydrochlorothiazide
Generic NameHydrochlorothiazide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1973-01-12
Marketing CategoryANDA / ANDA
Application NumberANDA083177
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 Through2019-12-31

Packaging

NDC 63629-6377-1

30 TABLET in 1 BOTTLE (63629-6377-1)
Marketing Start Date2015-08-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-6377-5 [63629637705]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA083177
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-02-15
Marketing End Date2019-12-31
Inactivation Date2020-01-31
Reactivation Date2020-05-22

NDC 63629-6377-3 [63629637703]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA083177
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-09-04
Marketing End Date2019-12-31
Inactivation Date2020-01-31
Reactivation Date2020-05-22

NDC 63629-6377-1 [63629637701]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA083177
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-08-21
Marketing End Date2019-12-31
Inactivation Date2020-01-31
Reactivation Date2020-05-22

NDC 63629-6377-2 [63629637702]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA083177
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-09-04
Marketing End Date2019-12-31
Inactivation Date2020-01-31
Reactivation Date2020-05-22

NDC 63629-6377-4 [63629637704]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA083177
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-08-26
Marketing End Date2019-12-31
Inactivation Date2020-01-31
Reactivation Date2020-05-22

Drug Details

Active Ingredients

IngredientStrength
HYDROCHLOROTHIAZIDE25 mg/1

OpenFDA Data

SPL SET ID:d31d570f-54b4-4d88-87b1-3604c0ddcdc9
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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