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    NDC 70518-1838-00 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 REMEDYREPACK INC.. The primary component is MIRTAZAPINE.

    Product Information

    NDC 70518-1838
    Product ID 70518-1838_036ebdc5-986d-a9d2-e063-6394a90ad55a
    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 15
    Active Ingredient Units mg/1
    Substance Name MIRTAZAPINE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076921
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-1838-00 (70518183800)

    NDC Package Code 70518-1838-0
    Billing NDC 70518183800
    Package 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1838-0)
    Marketing Start Date 2019-01-30
    NDC Exclude Flag N
    Pricing Information N/A