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    NDC 53002-1712-03 Mirtazapine 45 mg/1 Details

    Mirtazapine 45 mg/1

    Mirtazapine is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by RPK Pharmaceuticals, Inc.. The primary component is MIRTAZAPINE.

    Product Information

    NDC 53002-1712
    Product ID 53002-1712_a0a3ba9e-ebb6-4b3d-99da-a420eff6bced
    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 Mirtazapine
    Proprietary Name Suffix n/a
    Non-Proprietary Name Mirtazapine
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 45
    Active Ingredient Units mg/1
    Substance Name MIRTAZAPINE
    Labeler Name RPK Pharmaceuticals, Inc.
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077666
    Listing Certified Through 2024-12-31

    Package

    NDC 53002-1712-03 (53002171203)

    NDC Package Code 53002-1712-3
    Billing NDC 53002171203
    Package 30 TABLET, FILM COATED in 1 BOTTLE (53002-1712-3)
    Marketing Start Date 2018-10-01
    NDC Exclude Flag N
    Pricing Information N/A