Search by Drug Name or NDC

    NDC 17856-0595-04 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 ATLANTIC BIOLOGICALS CORP.. The primary component is ANHYDROUS CITRIC ACID; SODIUM CITRATE.

    Product Information

    NDC 17856-0595
    Product ID 17856-0595_c24a3a80-1e82-409b-bb4d-8e5e548fc00c
    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 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 ATLANTIC BIOLOGICALS CORP.
    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 2023-12-31

    Package

    NDC 17856-0595-04 (17856059504)

    NDC Package Code 17856-0595-4
    Billing NDC 17856059504
    Package 1 CASE in 1 CUP, UNIT-DOSE (17856-0595-4) / 50 CUP in 1 CASE (17856-0595-3) / 30 mL in 1 CUP
    Marketing Start Date 2022-09-02
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 42d837ae-2578-46df-92d2-24774964aaad Details

    Revised: 9/2022