Albumin (human) Solution
NDC Package 68982-643-01
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 68982-643 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
- 68982 - Octapharma Usa Inc
- 68982-643 - Albumin (human)
- 68982-643-01 - 50 mL in 1 BOTTLE, GLASS
- 68982-643 - 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.
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Billing & HCPCS Mapping
To facilitate insurance claims and reimbursement, this drug package is mapped to specific HCPCS administrative codes. This crosswalk aligns clinical data with the billing standards used in ASP (Average Sales Price), AWP, and OPPS payment systems. Use the cards below to identify the correct billable units for provider claims.
Note for Medical Coders: These mappings are synthesized from various CMS datasets including OPPS, PrEP, and DAC (Data Analysis and Coding) contractors. Always confirm unit conversions against the current quarter's pricing files before final submission.
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Other Available Packages
The following commercial packages are registered under the same Product NDC (68982-643). 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 68982-643-01 identifies a specific commercial package of 50 ml in 1 bottle, glass of Albumin (human), a plasma derivative labeled by Octapharma Usa Inc. This product is billed per "ML" milliliter and contains an estimated amount of 50 billable units per package. 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: 68982064301. 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.