Albumin (human)
NDC Package 67467-643-01
Package Information
Albumin (human) is do not use in individuals who are hypersensitive to albumin preparations, any ingredient in the formulation, or components of the container. Marketed by Octapharma Pharmazeutika Produktionsgesellschaft M.b.h., this product is identified by NDC 67467-643 and is authorized under FDA application BLA125154.
Identification & Billing
- RxCUI: 1741375 - albumin human 25 % in 50 ML Injection
- RxCUI: 1741375 - 50 ML albumin human, USP 250 MG/ML Injection
- RxCUI: 1741375 - albumin human 12.5 GM per 50 ML Injection
- RxCUI: 1741375 - albumin human 25 % per 50 ML Injection
- RxCUI: 1741380 - albumin human 25 % in 100 ML Injection
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 67467 - Octapharma Pharmazeutika Produktionsgesellschaft M.b.h.
- 67467-643 - Albumin (human)
- 67467-643-01 - 50 mL in 1 BOTTLE, GLASS
- 67467-643 - Albumin (human)
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 (67467-643). Click a package code to view its specific billing and regulatory data.
* 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 67467-643-01 identifies a specific commercial package of 50 ml in 1 bottle, glass of Albumin (human), labeled by Octapharma Pharmazeutika Produktionsgesellschaft M.b.h.. This product is billed per "ML" milliliter and contains an estimated amount of 50 billable units per package. This is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Octapharma Pharmazeutika Produktionsgesellschaft M.b.h. on October 17, 2006. The current certification is valid through December 31, 2017.
How is this Octapharma Pharmazeutika Produktionsgesellschaft M.b.h. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 67467064301. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. There are 50 total billable units per package. 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.