Search by Drug Name or NDC

    NDC 70518-1633-01 AMITRIPTYLINE HYDROCHLORIDE 50 mg/1 Details

    AMITRIPTYLINE HYDROCHLORIDE 50 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 70518-1633
    Product ID 70518-1633_030dd05a-e2d5-8d27-e063-6394a90a74c2
    Associated GPIs 58200010100315
    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 50
    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 70518-1633-01 (70518163301)

    NDC Package Code 70518-1633-1
    Billing NDC 70518163301
    Package 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1633-1)
    Marketing Start Date 2020-12-23
    NDC Exclude Flag N
    Pricing Information N/A