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    NDC 00002-8147-01 HUMATROPE Details

    HUMATROPE

    HUMATROPE is a INTRAMUSCULAR; SUBCUTANEOUS KIT in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Eli Lilly and Company. The primary component is .

    Product Information

    NDC 00002-8147
    Product ID 0002-8147_874d72c5-2ba2-409e-99c7-8e32f68b3dd4
    Associated GPIs
    GCN Sequence Number 029176
    GCN Sequence Number Description somatropin CARTRIDGE 6 MG INJECTION
    HIC3 P1A
    HIC3 Description GROWTH HORMONES
    GCN 25969
    HICL Sequence Number 002824
    HICL Sequence Number Description SOMATROPIN
    Brand/Generic Brand
    Proprietary Name HUMATROPE
    Proprietary Name Suffix n/a
    Non-Proprietary Name Somatropin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form KIT
    Route INTRAMUSCULAR; SUBCUTANEOUS
    Active Ingredient Strength n/a
    Active Ingredient Units n/a
    Substance Name n/a
    Labeler Name Eli Lilly and Company
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category BLA
    Application Number BLA019640
    Listing Certified Through 2024-12-31

    Package

    NDC 00002-8147-01 (00002814701)

    NDC Package Code 0002-8147-01
    Billing NDC 00002814701
    Package 1 TRAY in 1 CARTON (0002-8147-01) / 1 KIT in 1 TRAY * 2.88 mL in 1 CARTRIDGE (0002-7554-01) * 2.88 mL in 1 SYRINGE (0002-7618-01)
    Marketing Start Date 2006-01-27
    NDC Exclude Flag N
    Pricing Information N/A