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  5. NDC Package Code: 23731-6051-2 Anticoagulant Citrate Dextrose A

NDC Package 23731-6051-2 Anticoagulant Citrate Dextrose A

Anhydrous Citric Acid,Dextrose Monohydrate,And Trisodium Citrate Dihydrate Solution - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
23731-6051-2
Package Description:
25 VIAL, SINGLE-USE in 1 CASE / 30 mL in 1 VIAL, SINGLE-USE (23731-6051-3)
Product Code:
23731-6051
Proprietary Name:
Anticoagulant Citrate Dextrose A
Non-Proprietary Name:
Anhydrous Citric Acid, Dextrose Monohydrate, And Trisodium Citrate Dihydrate
Substance Name:
Anhydrous Citric Acid; Dextrose Monohydrate; Trisodium Citrate Dihydrate
Usage Information:
Anticoagulant Citrate Dextrose Solution, Solution A, U.S.P. (ACD-A), is intended for use as an anticoagulant in the extracorporeal blood processing with Autologous PRP Systems in production of platelet rich plasma (PRP). Refer to the manufacturer's Operator's Manual of the Autologous PRP System for the Directions for Use.
11-Digit NDC Billing Format:
23731605102
Product Type:
Human Prescription Drug
Labeler Name:
Citra Labs Llc
Dosage Form:
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route(s):
  • Extracorporeal - Administration outside of the body.
    • Active Ingredient(s):
  • ANHYDROUS CITRIC ACID .073 g/10mL
  • DEXTROSE MONOHYDRATE .245 g/10mL
  • TRISODIUM CITRATE DIHYDRATE .22 g/10mL
    • Pharmacologic Class(es):
  • Acidifying Activity - [MoA] (Mechanism of Action)
  • 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
    FDA Application Number:
    BN020037
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    08-26-2003
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    23731-6051-110 VIAL, SINGLE-USE in 1 CASE / 30 mL in 1 VIAL, SINGLE-USE (23731-6051-3)
    23731-6051-330 mL in 1 VIAL, SINGLE-USE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 23731-6051-2?

    The NDC Packaged Code 23731-6051-2 is assigned to a package of 25 vial, single-use in 1 case / 30 ml in 1 vial, single-use (23731-6051-3) of Anticoagulant Citrate Dextrose A, a human prescription drug labeled by Citra Labs Llc. The product's dosage form is solution and is administered via extracorporeal form.

    Is NDC 23731-6051 included in the NDC Directory?

    Yes, Anticoagulant Citrate Dextrose A with product code 23731-6051 is active and included in the NDC Directory. The product was first marketed by Citra Labs Llc on August 26, 2003 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 23731-6051-2?

    The 11-digit format is 23731605102. 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 5-4-1 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
    5-4-123731-6051-25-4-223731-6051-02