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    NDC 72786-0111-03 OXBRYTA 300 mg/1 Details

    OXBRYTA 300 mg/1

    OXBRYTA is a ORAL TABLET, FOR SUSPENSION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Global Blood Therapeutics, Inc, A subsidiary of Pfizer Inc.. The primary component is VOXELOTOR.

    Product Information

    NDC 72786-0111
    Product ID 72786-111_e27a3e07-438e-49d3-aae3-095e9379c7b4
    Associated GPIs 82805080007320
    GCN Sequence Number 082925
    GCN Sequence Number Description voxelotor TAB SUSP 300 MG ORAL
    HIC3 N1H
    HIC3 Description SICKLE CELL ANEMIA AGENTS
    GCN 51717
    HICL Sequence Number 046225
    HICL Sequence Number Description VOXELOTOR
    Brand/Generic Brand
    Proprietary Name OXBRYTA
    Proprietary Name Suffix n/a
    Non-Proprietary Name Voxelotor
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FOR SUSPENSION
    Route ORAL
    Active Ingredient Strength 300
    Active Ingredient Units mg/1
    Substance Name VOXELOTOR
    Labeler Name Global Blood Therapeutics, Inc, A subsidiary of Pfizer Inc.
    Pharmaceutical Class Cytochrome P450 3A4 Inhibitors [MoA], Hemoglobin S Polymerization Inhibitor [EPC], Hemoglobin S Polymerization Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA216157
    Listing Certified Through 2024-12-31

    Package

    NDC 72786-0111-03 (72786011103)

    NDC Package Code 72786-111-03
    Billing NDC 72786011103
    Package 90 TABLET, FOR SUSPENSION in 1 BOTTLE, PLASTIC (72786-111-03)
    Marketing Start Date 2021-12-17
    NDC Exclude Flag N
    Pricing Information N/A