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    NDC 70518-3034-00 Chlorpromazine hydrochloride 25 mg/1 Details

    Chlorpromazine hydrochloride 25 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 70518-3034
    Product ID 70518-3034_f6f2a55a-eccb-6145-e053-6394a90ab59b
    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 25
    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 ANDA213368
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-3034-00 (70518303400)

    NDC Package Code 70518-3034-0
    Billing NDC 70518303400
    Package 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3034-0)
    Marketing Start Date 2021-03-01
    NDC Exclude Flag N
    Pricing Information N/A