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    NDC 70518-1484-01 AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 Details

    AMITRIPTYLINE HYDROCHLORIDE 25 mg/1

    AMITRIPTYLINE 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 AMITRIPTYLINE HYDROCHLORIDE.

    Product Information

    NDC 70518-1484
    Product ID 70518-1484_f9c7a504-3ca7-b1db-e053-6394a90a9243
    Associated GPIs 58200010100310
    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 AMITRIPTYLINE HYDROCHLORIDE
    Proprietary Name Suffix n/a
    Non-Proprietary Name AMITRIPTYLINE HYDROCHLORIDE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 25
    Active Ingredient Units mg/1
    Substance Name AMITRIPTYLINE HYDROCHLORIDE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Tricyclic Antidepressant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202446
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-1484-01 (70518148401)

    NDC Package Code 70518-1484-1
    Billing NDC 70518148401
    Package 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1484-1)
    Marketing Start Date 2019-02-06
    NDC Exclude Flag N
    Pricing Information N/A