NDC 71335-0067

hydrochlorothiazide

Hydrochlorothiazide

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

Product ID71335-0067_68b6db12-2e6f-42f9-b182-de47ef502199
NDC71335-0067
Product TypeHuman Prescription Drug
Proprietary Namehydrochlorothiazide
Generic NameHydrochlorothiazide
Dosage FormCapsule
Route of AdministrationORAL
Marketing Start Date2010-03-15
Marketing CategoryANDA / ANDA
Application NumberANDA090510
Labeler NameBryant Ranch Prepack
Substance NameHYDROCHLOROTHIAZIDE
Active Ingredient Strength13 mg/1
Pharm ClassesIncreased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 71335-0067-1

30 CAPSULE in 1 BOTTLE (71335-0067-1)
Marketing Start Date2014-10-08
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0067-5 [71335006705]

hydrochlorothiazide CAPSULE
Marketing CategoryANDA
Application NumberANDA090510
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-10-08

NDC 71335-0067-7 [71335006707]

hydrochlorothiazide CAPSULE
Marketing CategoryANDA
Application NumberANDA090510
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-10-08

NDC 71335-0067-8 [71335006708]

hydrochlorothiazide CAPSULE
Marketing CategoryANDA
Application NumberANDA090510
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-10-08

NDC 71335-0067-2 [71335006702]

hydrochlorothiazide CAPSULE
Marketing CategoryANDA
Application NumberANDA090510
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-10-08

NDC 71335-0067-4 [71335006704]

hydrochlorothiazide CAPSULE
Marketing CategoryANDA
Application NumberANDA090510
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-10-08

NDC 71335-0067-1 [71335006701]

hydrochlorothiazide CAPSULE
Marketing CategoryANDA
Application NumberANDA090510
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-10-08

NDC 71335-0067-6 [71335006706]

hydrochlorothiazide CAPSULE
Marketing CategoryANDA
Application NumberANDA090510
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-10-08

NDC 71335-0067-3 [71335006703]

hydrochlorothiazide CAPSULE
Marketing CategoryANDA
Application NumberANDA090510
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-10-08

Drug Details

Active Ingredients

IngredientStrength
HYDROCHLOROTHIAZIDE12.5 mg/1

OpenFDA Data

SPL SET ID:6a11a458-dc69-40ba-a58a-649733e0e8ab
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 199903

    • 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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