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    NDC 68788-7683-06 Hydrochlorothiazide 12.5 mg/1 Details

    Hydrochlorothiazide 12.5 mg/1

    Hydrochlorothiazide is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is HYDROCHLOROTHIAZIDE.

    Product Information

    NDC 68788-7683
    Product ID 68788-7683_e984b63e-d6d4-4d20-b549-fc0ce4f6f3e6
    Associated GPIs 37600040000110
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Hydrochlorothiazide
    Proprietary Name Suffix n/a
    Non-Proprietary Name Hydrochlorothiazide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 12.5
    Active Ingredient Units mg/1
    Substance Name HYDROCHLOROTHIAZIDE
    Labeler Name Preferred Pharmaceuticals, Inc.
    Pharmaceutical Class Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203561
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7683-06 (68788768306)

    NDC Package Code 68788-7683-6
    Billing NDC 68788768306
    Package 60 CAPSULE in 1 BOTTLE (68788-7683-6)
    Marketing Start Date 2020-03-02
    NDC Exclude Flag N
    Pricing Information N/A