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  5. NDC Package Code: 13533-613-20 Plasmanate

NDC Package 13533-613-20 Plasmanate

Plasma Protein Fraction (human) 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:
13533-613-20
Package Description:
1 VIAL in 1 CARTON / 50 mL in 1 VIAL (13533-613-21)
Product Code:
13533-613
Proprietary Name:
Plasmanate
Non-Proprietary Name:
Plasma Protein Fraction (human)
Substance Name:
Albumin Human
Usage Information:
Treatment of Shock — Plasmanate is indicated in the treatment of shock due to burns, crushing injuries, abdominal emergencies, and any other cause where there is a predominant loss of plasma fluids and not red blood cells. It is also effective in the emergency treatment of shock due to hemorrhage.(3,4) Following the emergency phase of therapy, blood transfusions may be indicated depending on the severity of the blood loss.In infants and small children, Plasmanate has been found to be very useful in the initial therapy of shock due to dehydration and infection.
11-Digit NDC Billing Format:
13533061320
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1729438 - plasma protein fraction 2.5 GM in 50 ML (5 % ) Injection
  • RxCUI: 1729438 - 50 ML plasma protein fraction 50 MG/ML Injection
  • RxCUI: 1729438 - plasma protein fraction 2.5 GM per 50 ML Injection
  • RxCUI: 1729440 - Plasmanate 2.5 GM in 50 ML (5 % ) Injection
  • RxCUI: 1729440 - 50 ML plasma protein fraction 50 MG/ML Injection [Plasmanate]
    • Product Type:
    Plasma Derivative
    Labeler Name:
    Grifols Usa, 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):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • ALBUMIN HUMAN 2.5 g/50mL
    • Pharmacologic Class(es):
  • Human Serum Albumin - [EPC] (Established Pharmacologic Class)
  • Increased Intravascular Volume - [PE] (Physiologic Effect)
  • Increased Oncotic Pressure - [PE] (Physiologic Effect)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Serum Albumin - [Chemical/Ingredient]
    • Sample Package:
    No
    FDA Application Number:
    BLA101140
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    10-02-1958
    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
    13533-613-251 VIAL in 1 CARTON / 250 mL in 1 VIAL (13533-613-26)
    13533-613-271 VIAL in 1 CARTON / 500 mL in 1 VIAL (13533-613-28)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 13533-613-20?

    The NDC Packaged Code 13533-613-20 is assigned to a package of 1 vial in 1 carton / 50 ml in 1 vial (13533-613-21) of Plasmanate, a plasma derivative labeled by Grifols Usa, Llc. The product's dosage form is solution and is administered via intravenous form.

    Is NDC 13533-613 included in the NDC Directory?

    Yes, Plasmanate with product code 13533-613 is active and included in the NDC Directory. The product was first marketed by Grifols Usa, Llc on October 02, 1958 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 NDC billing unit for package 13533-613-20?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 13533-613-20?

    The 11-digit format is 13533061320. 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
    5-3-213533-613-205-4-213533-0613-20