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    NDC 68462-0865-10 Chlorpromazine Hydrochloride 200 mg/1 Details

    Chlorpromazine Hydrochloride 200 mg/1

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

    Product Information

    NDC 68462-0865
    Product ID 68462-865_7b80a6a5-1223-49ec-af0e-50f6584a77b7
    Associated GPIs 59200015100325
    GCN Sequence Number 003798
    GCN Sequence Number Description chlorpromazine HCl TABLET 200 MG ORAL
    HIC3 H2G
    HIC3 Description ANTIPSYCHOTICS,PHENOTHIAZINES
    GCN 14435
    HICL Sequence Number 001621
    HICL Sequence Number Description CHLORPROMAZINE HCL
    Brand/Generic Generic
    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 200
    Active Ingredient Units mg/1
    Substance Name CHLORPROMAZINE HYDROCHLORIDE
    Labeler Name Glenmark Pharmaceuticals Inc., USA
    Pharmaceutical Class Phenothiazine [EPC], Phenothiazines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA212144
    Listing Certified Through 2025-12-31

    Package

    NDC 68462-0865-10 (68462086510)

    NDC Package Code 68462-865-10
    Billing NDC 68462086510
    Package 1000 TABLET, FILM COATED in 1 BOTTLE (68462-865-10)
    Marketing Start Date 2021-03-23
    NDC Exclude Flag N
    Pricing Information N/A