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    NDC 70069-0816-10 Midazolam 2 mg/2mL Details

    Midazolam 2 mg/2mL

    Midazolam is a INTRAMUSCULAR; INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by SOMERSET THERAPEUTICS, LLC. The primary component is MIDAZOLAM HYDROCHLORIDE.

    Product Information

    NDC 70069-0816
    Product ID 70069-816_0bbe4e90-4c26-cbbb-e063-6294a90aad1b
    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 Midazolam
    Proprietary Name Suffix n/a
    Non-Proprietary Name midazolam hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION
    Route INTRAMUSCULAR; INTRAVENOUS
    Active Ingredient Strength 2
    Active Ingredient Units mg/2mL
    Substance Name MIDAZOLAM HYDROCHLORIDE
    Labeler Name SOMERSET THERAPEUTICS, LLC
    Pharmaceutical Class Benzodiazepine [EPC], Benzodiazepines [CS]
    DEA Schedule CIV
    Marketing Category ANDA
    Application Number ANDA090315
    Listing Certified Through 2024-12-31

    Package

    NDC 70069-0816-10 (70069081610)

    NDC Package Code 70069-816-10
    Billing NDC 70069081610
    Package 10 VIAL in 1 CARTON (70069-816-10) / 2 mL in 1 VIAL
    Marketing Start Date 2023-12-05
    NDC Exclude Flag N
    Pricing Information N/A