Search by Drug Name or NDC

    NDC 59651-0029-87 Lo-Zumandimine Details

    Lo-Zumandimine

    Lo-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 59651-0029
    Product ID 59651-029_7bc1835a-cc34-4b65-a6b5-f290aee806b4
    Associated GPIs 25990002150316
    GCN Sequence Number 060548
    GCN Sequence Number Description ethinyl estradiol/drospirenone TABLET 0.02-3(28) ORAL
    HIC3 G8A
    HIC3 Description CONTRACEPTIVES,ORAL
    GCN 26737
    HICL Sequence Number 022026
    HICL Sequence Number Description ETHINYL ESTRADIOL/DROSPIRENONE
    Brand/Generic Generic
    Proprietary Name Lo-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 ANDA209632
    Listing Certified Through 2024-12-31

    Package

    NDC 59651-0029-87 (59651002987)

    NDC Package Code 59651-029-87
    Billing NDC 59651002987
    Package 1 POUCH in 1 CARTON (59651-029-87) / 1 BLISTER PACK in 1 POUCH (59651-029-28) / 1 KIT in 1 BLISTER PACK
    Marketing Start Date 2018-02-27
    NDC Exclude Flag N
    Pricing Information N/A