Search by Drug Name or NDC

    NDC 70518-0016-00 Chlorpromazine Hydrochloride 50 mg/1 Details

    Chlorpromazine Hydrochloride 50 mg/1

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

    Product Information

    NDC 70518-0016
    Product ID 70518-0016_01f3ffdc-9a37-613b-e063-6294a90ac642
    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, SUGAR 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 ANDA084113
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-0016-00 (70518001600)

    NDC Package Code 70518-0016-0
    Billing NDC 70518001600
    Package 30 TABLET, SUGAR COATED in 1 BLISTER PACK (70518-0016-0)
    Marketing Start Date 2016-11-25
    NDC Exclude Flag N
    Pricing Information N/A