Albuked Solution
NDC Package 50090-6320-1
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 A-s Medication Solutions, this product is identified by NDC 50090-6320 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: 1742029 - albuked 25 % in 50 ML Injection
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 50090 - A-s Medication Solutions
- 50090-6320 - Albuked
- 50090-6320-1 - 25 VIAL in 1 CARTON / 50 mL in 1 VIAL (50090-6320-0)
- 50090-6320 - 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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 50090-6320-1 identifies a specific commercial package of 25 vial in 1 carton / 50 ml in 1 vial (50090-6320-0) of Albuked, a plasma derivative labeled by A-s Medication Solutions. 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 A-s Medication Solutions on October 21, 1942. The current certification is valid through December 31, 2026.
How is this A-s Medication Solutions product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 50090632001. 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 Package segment to maintain the 5-4-2 structure.