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    NDC 70710-1926-01 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 Zydus Pharmaceuticals USA Inc.. The primary component is SODIUM BENZOATE; SODIUM PHENYLACETATE.

    Product Information

    NDC 70710-1926
    Product ID 70710-1926_fd646c47-7fcd-4d60-8f6c-29e13f611c6d
    Associated GPIs
    GCN Sequence Number 058808
    GCN Sequence Number Description sodium benzoate/sod phenylacet VIAL 10 %-10 % INTRAVEN
    HIC3 D9A
    HIC3 Description AMMONIA INHIBITORS
    GCN 24322
    HICL Sequence Number 001398
    HICL Sequence Number Description SODIUM BENZOATE/SODIUM PHENYLACETATE
    Brand/Generic Generic
    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 Zydus Pharmaceuticals USA 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 ANDA217526
    Listing Certified Through 2024-12-31

    Package

    NDC 70710-1926-01 (70710192601)

    NDC Package Code 70710-1926-1
    Billing NDC 70710192601
    Package 1 VIAL in 1 CARTON (70710-1926-1) / 20 mL in 1 VIAL
    Marketing Start Date 2023-09-19
    NDC Exclude Flag N
    Pricing Information N/A