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    NDC 00078-0916-61 KISQALI FEMARA CO-PACK Details

    KISQALI FEMARA CO-PACK

    KISQALI FEMARA CO-PACK is a KIT in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Novartis Pharmaceuticals Corporation. The primary component is .

    Product Information

    NDC 00078-0916
    Product ID 0078-0916_5740112b-a7e5-47ec-955b-f25ad9c4344e
    Associated GPIs 2199000260B740
    GCN Sequence Number 077381
    GCN Sequence Number Description ribociclib succinate/letrozole TABLET 400-2.5 MG ORAL
    HIC3 V31
    HIC3 Description ANTINEOPLASTIC COMB - KINASE AND AROMATASE INHIBIT
    GCN 43368
    HICL Sequence Number 044246
    HICL Sequence Number Description RIBOCICLIB SUCCINATE/LETROZOLE
    Brand/Generic Brand
    Proprietary Name KISQALI FEMARA CO-PACK
    Proprietary Name Suffix n/a
    Non-Proprietary Name letrozole and ribociclib
    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 Novartis Pharmaceuticals Corporation
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA209935
    Listing Certified Through 2024-12-31

    Package

    NDC 00078-0916-61 (00078091661)

    NDC Package Code 0078-0916-61
    Billing NDC 00078091661
    Package 1 KIT in 1 KIT (0078-0916-61) * 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0078-0881-50) * 14 TABLET in 1 BLISTER PACK (0078-0895-14)
    Marketing Start Date 2017-05-04
    NDC Exclude Flag N
    Pricing Information N/A