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    NDC 70511-0101-50 SODIUM PHENYLACETATE AND SODIUM BENZOATE 100; 100 mg/mL; mg/mL Details

    SODIUM PHENYLACETATE AND SODIUM BENZOATE 100; 100 mg/mL; mg/mL

    SODIUM PHENYLACETATE AND SODIUM BENZOATE is a INTRAVENOUS INJECTION, SOLUTION, CONCENTRATE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by MAIA PHARMACEUTICALS, INC. The primary component is SODIUM BENZOATE; SODIUM PHENYLACETATE.

    Product Information

    NDC 70511-0101
    Product ID 70511-101_c158c088-1ab5-4099-a174-96aba96feb11
    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 SODIUM PHENYLACETATE AND SODIUM BENZOATE
    Proprietary Name Suffix n/a
    Non-Proprietary Name sodium phenylacetate and sodium benzoate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION, CONCENTRATE
    Route INTRAVENOUS
    Active Ingredient Strength 100; 100
    Active Ingredient Units mg/mL; mg/mL
    Substance Name SODIUM BENZOATE; SODIUM PHENYLACETATE
    Labeler Name MAIA PHARMACEUTICALS, INC
    Pharmaceutical Class Ammonium Ion Binding Activity [MoA], Ammonium Ion Binding Activity [MoA], Nitrogen Binding Agent [EPC], Nitrogen Binding Agent [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA208521
    Listing Certified Through 2024-12-31

    Package

    NDC 70511-0101-50 (70511010150)

    NDC Package Code 70511-101-50
    Billing NDC 70511010150
    Package 1 VIAL, SINGLE-DOSE in 1 CARTON (70511-101-50) / 50 mL in 1 VIAL, SINGLE-DOSE
    Marketing Start Date 2017-05-22
    NDC Exclude Flag N
    Pricing Information N/A
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