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    NDC 55292-0320-60 Isturisa 1 mg/1 Details

    Isturisa 1 mg/1

    Isturisa is a ORAL TABLET, COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Recordati Rare Diseases, Inc.. The primary component is OSILODROSTAT PHOSPHATE.

    Product Information

    NDC 55292-0320
    Product ID 55292-320_10dfb430-b311-4afe-9f28-e8cb47aa629a
    Associated GPIs 30022060600320
    GCN Sequence Number 080814
    GCN Sequence Number Description osilodrostat phosphate TABLET 1 MG ORAL
    HIC3 P1G
    HIC3 Description ADRENAL STEROID INHIBITORS
    GCN 47793
    HICL Sequence Number 046396
    HICL Sequence Number Description OSILODROSTAT PHOSPHATE
    Brand/Generic Brand
    Proprietary Name Isturisa
    Proprietary Name Suffix n/a
    Non-Proprietary Name Osilodrostat
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, COATED
    Route ORAL
    Active Ingredient Strength 1
    Active Ingredient Units mg/1
    Substance Name OSILODROSTAT PHOSPHATE
    Labeler Name Recordati Rare Diseases, Inc.
    Pharmaceutical Class Cortisol Synthesis Inhibitor [EPC], Cytochrome P450 11B1 Inhibitors [MoA], Cytochrome P450 1A2 Inhibitors [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Cytochrome P450 3A5 Inhibit
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA212801
    Listing Certified Through 2024-12-31

    Package

    NDC 55292-0320-60 (55292032060)

    NDC Package Code 55292-320-60
    Billing NDC 55292032060
    Package 60 TABLET, COATED in 1 BLISTER PACK (55292-320-60)
    Marketing Start Date 2020-03-31
    NDC Exclude Flag N
    Pricing Information N/A