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    NDC 71335-0122-05 Mirtazapine 15 mg/1 Details

    Mirtazapine 15 mg/1

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

    Product Information

    NDC 71335-0122
    Product ID 71335-0122_4a5e9ea6-3028-4765-94b7-fb10d6326eff
    Associated GPIs 58030050000315
    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 15
    Active Ingredient Units mg/1
    Substance Name MIRTAZAPINE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077666
    Listing Certified Through 2023-12-31

    Package

    NDC 71335-0122-05 (71335012205)

    NDC Package Code 71335-0122-5
    Billing NDC 71335012205
    Package 15 TABLET, FILM COATED in 1 BOTTLE (71335-0122-5)
    Marketing Start Date 2018-03-13
    NDC Exclude Flag N
    Pricing Information N/A