Albumin (human) Solution
NDC Package 68982-633-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Albumin (human) solution is do not use in individuals who are hypersensitive to albumin preparations, any ingredient in the formulation, or components of the container. This formulation utilizes a solution delivery system. Marketed by Octapharma Usa Inc, this product is identified by NDC 68982-633 and is authorized under FDA application BLA125154.

Identification & Billing

NDC Package Code
68982-633-01
Package Description
50 mL in 1 BOTTLE, GLASS
Product Code
68982-633
11-Digit Billing Format
68982063301
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Albumin (human)
Non-Proprietary Name
Albumin Human
Substance Name
Albumin Human
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
Intravenous - Administration within or into a vein or veins.
Active Ingredient(s)
ALBUMIN HUMAN 200 g/1000mL
Pharmacologic Class
Usage Information
Do not use in individuals who are hypersensitive to albumin preparations, any ingredient in the formulation, or components of the container.

Regulatory & Marketing

Labeler Name
Octapharma Usa Inc
Product Type
Plasma Derivative
FDA Application #
BLA125154
Marketing Category
BLA - A product marketed under an approved Biologic License Application.
Start Marketing Date
10-17-2006
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (68982-633). Click a package code to view its specific billing and regulatory data.

68982-633-02
100 mL in 1 BOTTLE, GLASS

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 68982-633-01 identifies a specific commercial package of 50 ml in 1 bottle, glass of Albumin (human), a plasma derivative labeled by Octapharma Usa Inc. This solution is formulated for intravenous use and contains albumin human as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Octapharma Usa Inc on October 17, 2006. The current certification is valid through December 31, 2026.

How is this Octapharma Usa Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 68982063301. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
68982-633-01
11-Digit CMS (5-4-2)
68982-0633-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.