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    NDC 00002-3002-01 MOUNJARO 15 mg/.5mL Details

    MOUNJARO 15 mg/.5mL

    MOUNJARO is a SUBCUTANEOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Eli Lilly and Company. The primary component is TIRZEPATIDE.

    Product Information

    NDC 00002-3002
    Product ID 0002-3002_b597917f-9673-4331-809d-79a538bb943c
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name MOUNJARO
    Proprietary Name Suffix n/a
    Non-Proprietary Name tirzepatide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION
    Route SUBCUTANEOUS
    Active Ingredient Strength 15
    Active Ingredient Units mg/.5mL
    Substance Name TIRZEPATIDE
    Labeler Name Eli Lilly and Company
    Pharmaceutical Class G-Protein-linked Receptor Interactions [MoA], GLP-1 Receptor Agonist [EPC], Glucagon-like Peptide-1 (GLP-1) Agonists [MoA], Glucose-dependent Insulinotropic Polypeptide Receptor Agonist [EPC]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA215866
    Listing Certified Through 2024-12-31

    Package

    NDC 00002-3002-01 (00002300201)

    NDC Package Code 0002-3002-01
    Billing NDC 00002300201
    Package 1 VIAL, SINGLE-DOSE in 1 CARTON (0002-3002-01) / .5 mL in 1 VIAL, SINGLE-DOSE
    Marketing Start Date 2023-07-28
    NDC Exclude Flag N
    Pricing Information N/A