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    NDC 62135-0630-30 CIMETIDINE 200 mg/1 Details

    CIMETIDINE 200 mg/1

    CIMETIDINE is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Chartwell RX, LLC. The primary component is CIMETIDINE.

    Product Information

    NDC 62135-0630
    Product ID 62135-630_0337689b-c5d5-d881-e063-6394a90aaec9
    Associated GPIs
    GCN Sequence Number 011665
    GCN Sequence Number Description cimetidine TABLET 200 MG ORAL
    HIC3 Z2D
    HIC3 Description HISTAMINE H2-RECEPTOR INHIBITORS
    GCN 46750
    HICL Sequence Number 004518
    HICL Sequence Number Description CIMETIDINE
    Brand/Generic Generic
    Proprietary Name CIMETIDINE
    Proprietary Name Suffix n/a
    Non-Proprietary Name CIMETIDINE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 200
    Active Ingredient Units mg/1
    Substance Name CIMETIDINE
    Labeler Name Chartwell RX, LLC
    Pharmaceutical Class Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA074329
    Listing Certified Through 2024-12-31

    Package

    NDC 62135-0630-30 (62135063030)

    NDC Package Code 62135-630-30
    Billing NDC 62135063030
    Package 30 TABLET, FILM COATED in 1 BOTTLE (62135-630-30)
    Marketing Start Date 2023-08-15
    NDC Exclude Flag N
    Pricing Information N/A