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    NDC 70518-3280-00 Chlorpromazine Hydrochloride 50 mg/1 Details

    Chlorpromazine Hydrochloride 50 mg/1

    Chlorpromazine Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is CHLORPROMAZINE HYDROCHLORIDE.

    Product Information

    NDC 70518-3280
    Product ID 70518-3280_f795e94e-106b-5d13-e053-6394a90a9bd7
    Associated GPIs
    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 Chlorpromazine Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Chlorpromazine Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 50
    Active Ingredient Units mg/1
    Substance Name CHLORPROMAZINE HYDROCHLORIDE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Phenothiazine [EPC], Phenothiazines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA212144
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-3280-00 (70518328000)

    NDC Package Code 70518-3280-0
    Billing NDC 70518328000
    Package 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3280-0)
    Marketing Start Date 2021-12-01
    NDC Exclude Flag N
    Pricing Information N/A