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    NDC 69784-0231-20 SODIUM ACETATE 164 mg/mL Details

    SODIUM ACETATE 164 mg/mL

    SODIUM ACETATE is a INTRAVENOUS INJECTION, SOLUTION, CONCENTRATE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Woodward Pharma Services LLC. The primary component is SODIUM ACETATE.

    Product Information

    NDC 69784-0231
    Product ID 69784-231_091ffeb5-7ec4-d28c-e063-6394a90a03c8
    Associated GPIs 79050010002005
    GCN Sequence Number 001205
    GCN Sequence Number Description sodium acetate VIAL 2 MEQ/ML INTRAVEN
    HIC3 C0K
    HIC3 Description BICARBONATE PRODUCING/CONTAINING AGENTS
    GCN 02922
    HICL Sequence Number 000536
    HICL Sequence Number Description SODIUM ACETATE
    Brand/Generic Generic
    Proprietary Name SODIUM ACETATE
    Proprietary Name Suffix n/a
    Non-Proprietary Name SODIUM ACETATE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION, CONCENTRATE
    Route INTRAVENOUS
    Active Ingredient Strength 164
    Active Ingredient Units mg/mL
    Substance Name SODIUM ACETATE
    Labeler Name Woodward Pharma Services LLC
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA214805
    Listing Certified Through 2024-12-31

    Package

    NDC 69784-0231-20 (69784023120)

    NDC Package Code 69784-231-20
    Billing NDC 69784023120
    Package 100 mL in 1 VIAL, PHARMACY BULK PACKAGE (69784-231-20)
    Marketing Start Date 2021-06-01
    NDC Exclude Flag N
    Pricing Information N/A