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    NDC 23155-0807-01 Chlorpromazine Hydrochloride 200 mg/1 Details

    Chlorpromazine Hydrochloride 200 mg/1

    Chlorpromazine Hydrochloride is a ORAL TABLET, COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.. The primary component is CHLORPROMAZINE HYDROCHLORIDE.

    Product Information

    NDC 23155-0807
    Product ID 23155-807_20d5cc4d-5a36-4a6e-9895-437936cd0e98
    Associated GPIs
    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, COATED
    Route ORAL
    Active Ingredient Strength 200
    Active Ingredient Units mg/1
    Substance Name CHLORPROMAZINE HYDROCHLORIDE
    Labeler Name Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
    Pharmaceutical Class Phenothiazine [EPC], Phenothiazines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA213590
    Listing Certified Through 2024-12-31

    Package

    NDC 23155-0807-01 (23155080701)

    NDC Package Code 23155-807-01
    Billing NDC 23155080701
    Package 100 TABLET, COATED in 1 BOTTLE (23155-807-01)
    Marketing Start Date 2023-06-25
    NDC Exclude Flag N
    Pricing Information N/A