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    NDC 00591-5715-01 Amoxapine 100 mg/1 Details

    Amoxapine 100 mg/1

    Amoxapine is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Actavis Pharma, Inc.. The primary component is AMOXAPINE.

    Product Information

    NDC 00591-5715
    Product ID 0591-5715_031890ec-0687-47cd-8046-6cdae8943311
    Associated GPIs 58200020000315
    GCN Sequence Number 046081
    GCN Sequence Number Description amoxapine TABLET 100 MG ORAL
    HIC3 H2U
    HIC3 Description TRICYCLIC ANTIDEPRESSANTS,REL.NON-SEL.REUPT-INHIB
    GCN 16557
    HICL Sequence Number 001648
    HICL Sequence Number Description AMOXAPINE
    Brand/Generic Generic
    Proprietary Name Amoxapine
    Proprietary Name Suffix n/a
    Non-Proprietary Name Amoxapine
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 100
    Active Ingredient Units mg/1
    Substance Name AMOXAPINE
    Labeler Name Actavis Pharma, Inc.
    Pharmaceutical Class Tricyclic Antidepressant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA072691
    Listing Certified Through 2024-12-31

    Package

    NDC 00591-5715-01 (00591571501)

    NDC Package Code 0591-5715-01
    Billing NDC 00591571501
    Package 100 TABLET in 1 BOTTLE, PLASTIC (0591-5715-01)
    Marketing Start Date 1992-08-28
    NDC Exclude Flag N
    Pricing Information N/A