1. Home
  2. Labeler Index
  3. Baxter Healthcare Corporation
  4. 24571-123
  5. NDC Package Code: 24571-123-02 Regiocit

NDC Package 24571-123-02 Regiocit

Sodium Chloride,Sodium Citrate Injection, Solution Extracorporeal - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
24571-123-02
Package Description:
2 BAG in 1 CARTON / 5000 mL in 1 BAG
Product Code:
24571-123
Proprietary Name:
Regiocit
Non-Proprietary Name:
Sodium Chloride, Sodium Citrate
Substance Name:
Sodium Chloride; Sodium Citrate, Unspecified Form
Usage Information:
Contraindications for the use of REGIOCIT include:•Severe liver failure•Shock with muscle hypoperfusion•Known hypersensitivity to any component of REGIOCIT REGIOCIT solution is contraindicated in:•patients who are hypersensitive to this drug or to any ingredient in the formulation, including any non-medicinal ingredient, or component of the container. For a complete listing, see Dosage Forms, Strengths, Composition and Packaging.•severe liver failure•shock with muscle hypoperfusion
11-Digit NDC Billing Format:
24571012302
NDC to RxNorm Crosswalk:
  • RxCUI: 2397251 - citrate 18 mmol / sodium 140 mmol in L Injection (EUA)
  • RxCUI: 2397251 - 5000 ML sodium chloride 5.03 MG/ML / sodium citrate 5.29 MG/ML Injection
  • RxCUI: 2397251 - 5000 ML NaCl 5.03 MG/ML / sodium citrate 5.29 MG/ML Injection
  • RxCUI: 2397251 - citrate 18 mmol / sodium 140 mmol per L Injection (EUA)
  • RxCUI: 2397257 - REGIOCIT (citrate 18 mmol / sodium 140 mmol in 1 L) 5000 ML Injection (EUA)
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Baxter Healthcare Corporation
    Dosage Form:
    Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
    Administration Route(s):
  • Extracorporeal - Administration outside of the body.
    • Active Ingredient(s):
  • SODIUM CHLORIDE 5.03 g/1000mL
  • SODIUM CITRATE, UNSPECIFIED FORM 5.29 g/1000mL
    • Pharmacologic Class(es):
  • Acidifying Activity - [MoA] (Mechanism of Action)
  • Anti-coagulant - [EPC] (Established Pharmacologic Class)
  • Calcium Chelating Activity - [MoA] (Mechanism of Action)
  • Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
  • Decreased Coagulation Factor Activity - [PE] (Physiologic Effect)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    09-18-2020
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 24571-123-02?

    The NDC Packaged Code 24571-123-02 is assigned to a package of 2 bag in 1 carton / 5000 ml in 1 bag of Regiocit, a human prescription drug labeled by Baxter Healthcare Corporation. The product's dosage form is injection, solution and is administered via extracorporeal form.

    Is NDC 24571-123 included in the NDC Directory?

    Yes, Regiocit with product code 24571-123 is active and included in the NDC Directory. The product was first marketed by Baxter Healthcare Corporation on September 18, 2020 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 24571-123-02?

    The 11-digit format is 24571012302. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-224571-123-025-4-224571-0123-02