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  5. NDC Package Code: 61953-0001-2 Human Albumin Grifols

NDC Package 61953-0001-2 Human Albumin Grifols

Albumin (human) Solution Intravenous - 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:
61953-0001-2
Package Description:
1 VIAL in 1 CARTON / 100 mL in 1 VIAL (61953-0001-4)
Product Code:
61953-0001
Proprietary Name:
Human Albumin Grifols
Non-Proprietary Name:
Albumin (human)
Substance Name:
Albumin Human
Usage Information:
Hypersensitivity to albumin preparations or to any of the excipients.Severe anemia or cardiac failure with normal or increased intravascular volume.
11-Digit NDC Billing Format:
61953000102
NDC to RxNorm Crosswalk:
  • RxCUI: 1741295 - albumin human 20 % in 100 ML Injection
  • RxCUI: 1741295 - 100 ML albumin human, USP 200 MG/ML Injection
  • RxCUI: 1741295 - albumin human 20 % per 100 ML Injection
  • RxCUI: 1741295 - albumin human 20 GM per 100 ML Injection
  • RxCUI: 1741304 - Human Albumin Grifols 20 % in 100 ML Injection
    • 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 10 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:
    BLA103352
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    02-17-1995
    Listing Expiration Date:
    12-31-2025
    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 61953-0001-2?

    The NDC Packaged Code 61953-0001-2 is assigned to a package of 1 vial in 1 carton / 100 ml in 1 vial (61953-0001-4) of Human Albumin Grifols, a plasma derivative labeled by Grifols Usa, Llc. The product's dosage form is solution and is administered via intravenous form.

    Is NDC 61953-0001 included in the NDC Directory?

    Yes, Human Albumin Grifols with product code 61953-0001 is active and included in the NDC Directory. The product was first marketed by Grifols Usa, Llc on February 17, 1995 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 61953-0001-2?

    The 11-digit format is 61953000102. 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
    5-4-161953-0001-25-4-261953-0001-02