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    NDC 51655-0121-26 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 Northwind Pharmaceuticals. The primary component is AMITRIPTYLINE HYDROCHLORIDE.

    Product Information

    NDC 51655-0121
    Product ID 51655-121_f304d8da-3d24-7ca8-e053-2a95a90ab772
    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 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 Northwind Pharmaceuticals
    Pharmaceutical Class Tricyclic Antidepressant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202446
    Listing Certified Through 2024-12-31

    Package

    NDC 51655-0121-26 (51655012126)

    NDC Package Code 51655-121-26
    Billing NDC 51655012126
    Package 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-121-26)
    Marketing Start Date 2022-08-10
    NDC Exclude Flag N
    Pricing Information N/A