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    NDC 70518-2258-00 AMITRIPTYLINE HYDROCHLORIDE 150 mg/1 Details

    AMITRIPTYLINE HYDROCHLORIDE 150 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 70518-2258
    Product ID 70518-2258_0386afa4-b465-6e2a-e063-6294a90a1ecc
    Associated GPIs 58200010100330
    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 150
    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 70518-2258-00 (70518225800)

    NDC Package Code 70518-2258-0
    Billing NDC 70518225800
    Package 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2258-0)
    Marketing Start Date 2019-08-09
    NDC Exclude Flag N
    Pricing Information N/A