Search by Drug Name or NDC

    NDC 71151-0025-01 Mycophenolate Mofetil 200 mg/mL Details

    Mycophenolate Mofetil 200 mg/mL

    Mycophenolate Mofetil is a ORAL POWDER, FOR SUSPENSION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by airis PHARMA Private Limited. The primary component is MYCOPHENOLATE MOFETIL.

    Product Information

    NDC 71151-0025
    Product ID 71151-025_0ef7f20f-a14b-448e-8d10-5e902056b1db
    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 Mycophenolate Mofetil
    Proprietary Name Suffix n/a
    Non-Proprietary Name Mycophenolate Mofetil
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form POWDER, FOR SUSPENSION
    Route ORAL
    Active Ingredient Strength 200
    Active Ingredient Units mg/mL
    Substance Name MYCOPHENOLATE MOFETIL
    Labeler Name airis PHARMA Private Limited
    Pharmaceutical Class Antimetabolite Immunosuppressant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA213955
    Listing Certified Through 2024-12-31

    Package

    NDC 71151-0025-01 (71151002501)

    NDC Package Code 71151-025-01
    Billing NDC 71151002501
    Package 1 BOTTLE, PLASTIC in 1 CARTON (71151-025-01) / 225 mL in 1 BOTTLE, PLASTIC
    Marketing Start Date 2023-09-22
    NDC Exclude Flag N
    Pricing Information N/A