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    NDC 68788-7754-03 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 Preferred Pharmaceuticals, Inc.. The primary component is MIRTAZAPINE.

    Product Information

    NDC 68788-7754
    Product ID 68788-7754_6ccb8f08-9d9e-4f1a-b22f-5e92644ea125
    Associated GPIs 58030050000345
    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 Preferred Pharmaceuticals, Inc.
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076921
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7754-03 (68788775403)

    NDC Package Code 68788-7754-3
    Billing NDC 68788775403
    Package 30 TABLET, FILM COATED in 1 BOTTLE (68788-7754-3)
    Marketing Start Date 2020-07-01
    NDC Exclude Flag N
    Pricing Information N/A