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    NDC 58407-0625-06 STAHIST AD 25; 60 mg/1; mg/1 Details

    STAHIST AD 25; 60 mg/1; mg/1

    STAHIST AD is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Magna Pharmaceuticals, Inc.. The primary component is CHLORCYCLIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE.

    Product Information

    NDC 58407-0625
    Product ID 58407-625_07737712-83d6-fd68-e063-6294a90a4b5c
    Associated GPIs 43993002280320
    GCN Sequence Number 068279
    GCN Sequence Number Description chlorcyclizine/pseudoephedrine TABLET 25 MG-60MG ORAL
    HIC3 Z2N
    HIC3 Description 1ST GEN ANTIHISTAMINE AND DECONGESTANT COMBINATION
    GCN 31036
    HICL Sequence Number 037465
    HICL Sequence Number Description CHLORCYCLIZINE HCL/PSEUDOEPHEDRINE HCL
    Brand/Generic Brand
    Proprietary Name STAHIST AD
    Proprietary Name Suffix n/a
    Non-Proprietary Name CHLORCYCLIZINE HYDROCHLORIDE and PSEUDOEPHEDRINE HYDROCHLORIDE
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 25; 60
    Active Ingredient Units mg/1; mg/1
    Substance Name CHLORCYCLIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
    Labeler Name Magna Pharmaceuticals, Inc.
    Pharmaceutical Class Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH DRUG
    Application Number M012
    Listing Certified Through 2024-12-31

    Package

    NDC 58407-0625-06 (58407062506)

    NDC Package Code 58407-625-06
    Billing NDC 58407062506
    Package 6 BLISTER PACK in 1 BOX (58407-625-06) / 1 TABLET in 1 BLISTER PACK (58407-625-01)
    Marketing Start Date 2011-12-20
    NDC Exclude Flag N
    Pricing Information N/A