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  5. NDC Package Code: 53157-136-94 Leukotrap Wb System

NDC Package 53157-136-94 Leukotrap Wb System

Cpda-1 Blood Bag Collection System Solution Intravenous - 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:
53157-136-94
Package Description:
18 BAG in 1 CARTON / 70 mL in 1 BAG
Product Code:
53157-136
Proprietary Name:
Leukotrap Wb System
Non-Proprietary Name:
Cpda-1 Blood Bag Collection System
Substance Name:
Adenine; Citric Acid Monohydrate; Dextrose Monohydrate; Sodium Citrate; Sodium Phosphate, Monobasic, Monohydrate
Usage Information:
Indicated for collection of blood and preparation of red blood cells and plasma with pre-storage leukocyte reduction. Platelet concentrates are not intended to be made with this product.
11-Digit NDC Billing Format:
53157013694
Product Type:
Human Prescription Drug
Labeler Name:
Haemonetics Corporation
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):
  • Intravenous - Administration within or into a vein or veins.
  • Intravenous - Administration within or into a vein or veins.
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • ADENINE .019 g/70mL
  • CITRIC ACID MONOHYDRATE .229 g/70mL
  • DEXTROSE MONOHYDRATE 2.23 g/70mL
  • SODIUM CITRATE 1.84 g/70mL
  • SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE .155 g/70mL
  • ADENINE .019 g/70mL
  • CITRIC ACID MONOHYDRATE .229 g/70mL
  • DEXTROSE MONOHYDRATE 2.23 g/70mL
  • SODIUM CITRATE 1.84 g/70mL
  • SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE .155 g/70mL
  • ADENINE .019 g/70mL
  • CITRIC ACID MONOHYDRATE .229 g/70mL
  • DEXTROSE MONOHYDRATE 2.23 g/70mL
  • SODIUM CITRATE 1.84 g/70mL
  • SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE .155 g/70mL
    • 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)
  • 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)
  • 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:
    BN800077
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    11-06-1980
    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
    53157-136-9270 mL in 1 BAG
    53157-136-9318 BAG in 1 CARTON / 70 mL in 1 BAG

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 53157-136-94?

    The NDC Packaged Code 53157-136-94 is assigned to a package of 18 bag in 1 carton / 70 ml in 1 bag of Leukotrap Wb System, a human prescription drug labeled by Haemonetics Corporation. The product's dosage form is solution and is administered via intravenous form.

    Is NDC 53157-136 included in the NDC Directory?

    Yes, Leukotrap Wb System with product code 53157-136 is active and included in the NDC Directory. The product was first marketed by Haemonetics Corporation on November 06, 1980 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 53157-136-94?

    The 11-digit format is 53157013694. 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
    5-3-253157-136-945-4-253157-0136-94