NDC 12634-471

HYDROCHLOROTHIAZIDE

Hydrochlorothiazide

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

Product ID12634-471_f603db60-428d-470d-96d6-2c9486dfa784
NDC12634-471
Product TypeHuman Prescription Drug
Proprietary NameHYDROCHLOROTHIAZIDE
Generic NameHydrochlorothiazide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2009-06-30
Marketing CategoryANDA / ANDA
Application NumberANDA084324
Labeler NameApotheca, Inc.
Substance NameHYDROCHLOROTHIAZIDE
Active Ingredient Strength50 mg/1
Pharm ClassesIncreased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 12634-471-91

1 TABLET in 1 BLISTER PACK (12634-471-91)
Marketing Start Date2009-06-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 12634-471-91 [12634047191]

HYDROCHLOROTHIAZIDE TABLET
Marketing CategoryANDA
Application NumberANDA084324
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-06-30
Inactivation Date2020-01-31

NDC 12634-471-85 [12634047185]

HYDROCHLOROTHIAZIDE TABLET
Marketing CategoryANDA
Application NumberANDA084324
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-06-30
Inactivation Date2020-01-31

NDC 12634-471-79 [12634047179]

HYDROCHLOROTHIAZIDE TABLET
Marketing CategoryANDA
Application NumberANDA084324
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-06-30
Inactivation Date2020-01-31

NDC 12634-471-90 [12634047190]

HYDROCHLOROTHIAZIDE TABLET
Marketing CategoryANDA
Application NumberANDA084324
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-06-30
Inactivation Date2020-01-31

NDC 12634-471-78 [12634047178]

HYDROCHLOROTHIAZIDE TABLET
Marketing CategoryANDA
Application NumberANDA084324
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-06-30
Inactivation Date2020-01-31

NDC 12634-471-50 [12634047150]

HYDROCHLOROTHIAZIDE TABLET
Marketing CategoryANDA
Application NumberANDA084324
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-06-30
Inactivation Date2020-01-31

NDC 12634-471-71 [12634047171]

HYDROCHLOROTHIAZIDE TABLET
Marketing CategoryANDA
Application NumberANDA084324
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-06-30
Inactivation Date2020-01-31

NDC 12634-471-60 [12634047160]

HYDROCHLOROTHIAZIDE TABLET
Marketing CategoryANDA
Application NumberANDA084324
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-06-30
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
HYDROCHLOROTHIAZIDE50 mg/1

OpenFDA Data

SPL SET ID:2c4954a3-35dd-4ea1-ad32-0044d6db1665
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
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.