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    NDC 53002-1270-03 Mirtazapine 30 mg/1 Details

    Mirtazapine 30 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 53002-1270
    Product ID 53002-1270_2c8c65d0-8f32-4ca2-9632-216948261cf3
    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 30
    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 ANDA076921
    Listing Certified Through 2024-12-31

    Package

    NDC 53002-1270-03 (53002127003)

    NDC Package Code 53002-1270-3
    Billing NDC 53002127003
    Package 30 TABLET, FILM COATED in 1 BOTTLE (53002-1270-3)
    Marketing Start Date 2022-07-01
    NDC Exclude Flag N
    Pricing Information N/A