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    NDC 62135-0700-90 Amoxapine 25 mg/1 Details

    Amoxapine 25 mg/1

    Amoxapine is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Chartwell RX, LLC. The primary component is AMOXAPINE.

    Product Information

    NDC 62135-0700
    Product ID 62135-700_04de67ce-c87b-d4bd-e063-6294a90a4392
    Associated GPIs
    GCN Sequence Number 046083
    GCN Sequence Number Description amoxapine TABLET 25 MG ORAL
    HIC3 H2U
    HIC3 Description TRICYCLIC ANTIDEPRESSANTS,REL.NON-SEL.REUPT-INHIB
    GCN 16559
    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 25
    Active Ingredient Units mg/1
    Substance Name AMOXAPINE
    Labeler Name Chartwell RX, LLC
    Pharmaceutical Class Tricyclic Antidepressant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA072943
    Listing Certified Through 2024-12-31

    Package

    NDC 62135-0700-90 (62135070090)

    NDC Package Code 62135-700-90
    Billing NDC 62135070090
    Package 90 TABLET in 1 BOTTLE (62135-700-90)
    Marketing Start Date 2023-09-06
    NDC Exclude Flag N
    Pricing Information N/A