NDC 0615-1358

Hydrochlorothiazide

Hydrochlorothiazide

Hydrochlorothiazide is a Oral Capsule, Gelatin Coated in the Human Prescription Drug category. It is labeled and distributed by Ncs Healthcare Of Ky, Inc Dba Vangard Labs. The primary component is Hydrochlorothiazide.

Product ID0615-1358_96e5457c-c9e8-47f9-bcec-a530cf80969a
NDC0615-1358
Product TypeHuman Prescription Drug
Proprietary NameHydrochlorothiazide
Generic NameHydrochlorothiazide
Dosage FormCapsule, Gelatin Coated
Route of AdministrationORAL
Marketing Start Date1996-12-27
Marketing CategoryNDA AUTHORIZED GENERIC / NDA AUTHORIZED GENERIC
Application NumberNDA020504
Labeler NameNCS HealthCare of KY, Inc dba Vangard Labs
Substance NameHYDROCHLOROTHIAZIDE
Active Ingredient Strength13 mg/1
Pharm ClassesIncreased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 0615-1358-30

6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-1358-30) > 5 CAPSULE, GELATIN COATED in 1 BLISTER PACK
Marketing Start Date1996-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0615-1358-31 [00615135831]

Hydrochlorothiazide CAPSULE, GELATIN COATED
Marketing CategoryNDA AUTHORIZED GENERIC
Application NumberNDA020504
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1996-12-27
Inactivation Date2020-01-31

NDC 0615-1358-30 [00615135830]

Hydrochlorothiazide CAPSULE, GELATIN COATED
Marketing CategoryNDA AUTHORIZED GENERIC
Application NumberNDA020504
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-01-07
Inactivation Date2020-01-31

NDC 0615-1358-14 [00615135814]

Hydrochlorothiazide CAPSULE, GELATIN COATED
Marketing CategoryNDA AUTHORIZED GENERIC
Application NumberNDA020504
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-05-20
Inactivation Date2020-01-31

NDC 0615-1358-05 [00615135805]

Hydrochlorothiazide CAPSULE, GELATIN COATED
Marketing CategoryNDA AUTHORIZED GENERIC
Application NumberNDA020504
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1996-12-27
Inactivation Date2020-01-31

NDC 0615-1358-39 [00615135839]

Hydrochlorothiazide CAPSULE, GELATIN COATED
Marketing CategoryNDA AUTHORIZED GENERIC
Application NumberNDA020504
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1996-12-27
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
HYDROCHLOROTHIAZIDE12.5 mg/1

OpenFDA Data

SPL SET ID:3b369a4b-8316-4d27-abc8-e8eecee079e2
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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