Search by Drug Name or NDC

    NDC 68788-7982-03 Meclizine HCL 25 mg 25 mg/1 Details

    Meclizine HCL 25 mg 25 mg/1

    Meclizine HCL 25 mg is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is MECLIZINE HYDROCHLORIDE.

    Product Information

    NDC 68788-7982
    Product ID 68788-7982_7a562594-c818-445c-a456-131c699b97b7
    Associated GPIs 50200050000510
    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 Meclizine HCL 25 mg
    Proprietary Name Suffix n/a
    Non-Proprietary Name Meclizine HCL
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 25
    Active Ingredient Units mg/1
    Substance Name MECLIZINE HYDROCHLORIDE
    Labeler Name Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Antiemetic [EPC], Emesis Suppression [PE]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part336
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7982-03 (68788798203)

    NDC Package Code 68788-7982-3
    Billing NDC 68788798203
    Package 30 TABLET in 1 BOTTLE, PLASTIC (68788-7982-3)
    Marketing Start Date 2021-07-28
    NDC Exclude Flag N
    Pricing Information N/A