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    NDC 00591-5716-30 Amoxapine 150 mg/1 Details

    Amoxapine 150 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 00591-5716
    Product ID 0591-5716_031890ec-0687-47cd-8046-6cdae8943311
    Associated GPIs 58200020000320
    GCN Sequence Number 046082
    GCN Sequence Number Description amoxapine TABLET 150 MG ORAL
    HIC3 H2U
    HIC3 Description TRICYCLIC ANTIDEPRESSANTS,REL.NON-SEL.REUPT-INHIB
    GCN 16558
    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 150
    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 00591-5716-30 (00591571630)

    NDC Package Code 0591-5716-30
    Billing NDC 00591571630
    Package 30 TABLET in 1 BOTTLE, PLASTIC (0591-5716-30)
    Marketing Start Date 1992-08-28
    NDC Exclude Flag N
    Pricing Information N/A