Albuked Solution
NDC Package 76125-792-10
Package Information
Albuked (albumin (human)) solution is emergency Treatment of Hypovolemic ShockAlbuked 25 is hyperoncotic and on intravenous infusion will expand the plasma volume by an additional amount, three to four times the volume actually administered, by withdrawing fluid from the interstitial spaces, provided the patient is normally hydrated interstitially or there is interstitial edema.(1) If the patient is dehydrated, additional crystalloids must be given,(4) or alternatively, Albumin (Human) 5%, USP (Albuked™ 5) should be used. This formulation utilizes a solution delivery system. Marketed by Kedrion Biopharma, Inc., this product is identified by NDC 76125-792 and is authorized under FDA application BLA101138.
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
- 76125 - Kedrion Biopharma, Inc.
- 76125-792 - Albuked
- 76125-792-10 - 1 VIAL in 1 CARTON / 100 mL in 1 VIAL (76125-792-11)
- 76125-792 - Albuked
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 (76125-792). 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 76125-792-10 identifies a specific commercial package of 1 vial in 1 carton / 100 ml in 1 vial (76125-792-11) of Albuked, a plasma derivative labeled by Kedrion Biopharma, 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 Kedrion Biopharma, Inc. on October 21, 1942. The current certification is valid through December 31, 2026.
How is this Kedrion Biopharma, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 76125079210. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. 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.