NDC 68788-9867

Hydrochlorothiazide

Hydrochlorothiazide

Hydrochlorothiazide is a Oral Capsule, Gelatin Coated in the Human Prescription Drug category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is Hydrochlorothiazide.

Product ID68788-9867_abf822a1-6864-444f-8066-6edd1b644d14
NDC68788-9867
Product TypeHuman Prescription Drug
Proprietary NameHydrochlorothiazide
Generic NameHydrochlorothiazide
Dosage FormCapsule, Gelatin Coated
Route of AdministrationORAL
Marketing Start Date2015-08-14
Marketing CategoryNDA AUTHORIZED GENERIC / NDA AUTHORIZED GENERIC
Application NumberNDA020504
Labeler NamePreferred Pharmaceuticals Inc.
Substance NameHYDROCHLOROTHIAZIDE
Active Ingredient Strength13 mg/1
Pharm ClassesIncreased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 68788-9867-3

30 CAPSULE, GELATIN COATED in 1 BOTTLE (68788-9867-3)
Marketing Start Date2015-08-14
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-9867-9 [68788986709]

Hydrochlorothiazide CAPSULE, GELATIN COATED
Marketing CategoryNDA authorized generic
Application NumberNDA020504
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-08-14
Marketing End Date2019-12-06

NDC 68788-9867-6 [68788986706]

Hydrochlorothiazide CAPSULE, GELATIN COATED
Marketing CategoryNDA authorized generic
Application NumberNDA020504
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-08-14
Marketing End Date2019-12-06

NDC 68788-9867-1 [68788986701]

Hydrochlorothiazide CAPSULE, GELATIN COATED
Marketing CategoryNDA authorized generic
Application NumberNDA020504
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-08-14
Marketing End Date2019-12-06

NDC 68788-9867-8 [68788986708]

Hydrochlorothiazide CAPSULE, GELATIN COATED
Marketing CategoryNDA authorized generic
Application NumberNDA020504
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-08-14
Marketing End Date2019-12-06

NDC 68788-9867-3 [68788986703]

Hydrochlorothiazide CAPSULE, GELATIN COATED
Marketing CategoryNDA authorized generic
Application NumberNDA020504
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-08-14
Marketing End Date2019-12-06

Drug Details

Active Ingredients

IngredientStrength
HYDROCHLOROTHIAZIDE12.5 mg/1

OpenFDA Data

SPL SET ID:f8bf8cf0-df94-4fe1-afc4-a105bbd337df
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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