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    NDC 59651-0030-87 Zumandimine Details

    Zumandimine

    Zumandimine is a KIT in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Aurobindo Pharma Limited. The primary component is .

    Product Information

    NDC 59651-0030
    Product ID 59651-030_7cec3990-8d5f-4585-8bbc-fe2556cf69f5
    Associated GPIs 25990002150320
    GCN Sequence Number 047787
    GCN Sequence Number Description ethinyl estradiol/drospirenone TABLET 0.03MG-3MG ORAL
    HIC3 G8A
    HIC3 Description CONTRACEPTIVES,ORAL
    GCN 13083
    HICL Sequence Number 022026
    HICL Sequence Number Description ETHINYL ESTRADIOL/DROSPIRENONE
    Brand/Generic Generic
    Proprietary Name Zumandimine
    Proprietary Name Suffix n/a
    Non-Proprietary Name Drospirenone and Ethinyl Estradiol
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form KIT
    Route n/a
    Active Ingredient Strength n/a
    Active Ingredient Units n/a
    Substance Name n/a
    Labeler Name Aurobindo Pharma Limited
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA209407
    Listing Certified Through 2024-12-31

    Package

    NDC 59651-0030-87 (59651003087)

    NDC Package Code 59651-030-87
    Billing NDC 59651003087
    Package 1 POUCH in 1 CARTON (59651-030-87) / 1 BLISTER PACK in 1 POUCH / 1 KIT in 1 BLISTER PACK
    Marketing Start Date 2018-03-26
    NDC Exclude Flag N
    Pricing Information N/A