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    NDC 69660-0202-91 Rubraca 250 mg/1 Details

    Rubraca 250 mg/1

    Rubraca is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Clovis Oncology, Inc.. The primary component is RUCAPARIB CAMSYLATE.

    Product Information

    NDC 69660-0202
    Product ID 69660-202_0aeb47f7-f854-e93d-e063-6394a90a4350
    Associated GPIs 21535570200325
    GCN Sequence Number 077432
    GCN Sequence Number Description rucaparib camsylate TABLET 250 MG ORAL
    HIC3 V1Q
    HIC3 Description ANTINEOPLASTIC SYSTEMIC ENZYME INHIBITORS
    GCN 43453
    HICL Sequence Number 044002
    HICL Sequence Number Description RUCAPARIB CAMSYLATE
    Brand/Generic Brand
    Proprietary Name Rubraca
    Proprietary Name Suffix n/a
    Non-Proprietary Name rucaparib
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 250
    Active Ingredient Units mg/1
    Substance Name RUCAPARIB CAMSYLATE
    Labeler Name Clovis Oncology, Inc.
    Pharmaceutical Class Poly(ADP-Ribose) Polymerase Inhibitor [EPC], Poly(ADP-Ribose) Polymerase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA209115
    Listing Certified Through 2024-12-31

    Package

    NDC 69660-0202-91 (69660020291)

    NDC Package Code 69660-202-91
    Billing NDC 69660020291
    Package 60 TABLET, FILM COATED in 1 BOTTLE (69660-202-91)
    Marketing Start Date 2017-05-01
    NDC Exclude Flag N
    Pricing Information N/A