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    NDC 00121-0595-00 Sodium Citrate and Citric Acid 334; 500 mg/5mL; mg/5mL Details

    Sodium Citrate and Citric Acid 334; 500 mg/5mL; mg/5mL

    Sodium Citrate and Citric Acid is a ORAL SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Pharmaceutical Associates, Inc.. The primary component is ANHYDROUS CITRIC ACID; SODIUM CITRATE.

    Product Information

    NDC 00121-0595
    Product ID 0121-0595_efe0dd73-00d4-9223-e053-2a95a90a1bae
    Associated GPIs 56202020002010
    GCN Sequence Number 043912
    GCN Sequence Number Description citric acid/sodium citrate SOLUTION 334-500MG ORAL
    HIC3 R1S
    HIC3 Description URINARY PH MODIFIERS
    GCN 51957
    HICL Sequence Number 003682
    HICL Sequence Number Description CITRIC ACID/SODIUM CITRATE
    Brand/Generic Generic
    Proprietary Name Sodium Citrate and Citric Acid
    Proprietary Name Suffix n/a
    Non-Proprietary Name SODIUM CITRATE and CITRIC ACID MONOHYDRATE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form SOLUTION
    Route ORAL
    Active Ingredient Strength 334; 500
    Active Ingredient Units mg/5mL; mg/5mL
    Substance Name ANHYDROUS CITRIC ACID; SODIUM CITRATE
    Labeler Name Pharmaceutical Associates, Inc.
    Pharmaceutical Class Acidifying Activity [MoA], Acidifying Activity [MoA], Anti-coagulant [EPC], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Calculi Dissolution Agent [EPC], Decreased Coagulation F
    DEA Schedule n/a
    Marketing Category UNAPPROVED DRUG OTHER
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 00121-0595-00 (00121059500)

    NDC Package Code 0121-0595-00
    Billing NDC 00121059500
    Package 10 TRAY in 1 CASE (0121-0595-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (0121-0595-15)
    Marketing Start Date 1969-01-01
    NDC Exclude Flag N
    Pricing Information N/A