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    NDC 68788-7251-06 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 Preferred Pharmaceuticals Inc.. The primary component is MIRTAZAPINE.

    Product Information

    NDC 68788-7251
    Product ID 68788-7251_7b33d4be-2695-4b20-bc7f-0b723c18ca4c
    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 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 68788-7251-06 (68788725106)

    NDC Package Code 68788-7251-6
    Billing NDC 68788725106
    Package 60 TABLET, FILM COATED in 1 BOTTLE (68788-7251-6)
    Marketing Start Date 2018-08-28
    NDC Exclude Flag N
    Pricing Information N/A