Octagam Immune Globulin (human) Solution
NDC Package 68982-840-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Octagam Immune Globulin (human) (immune globulin) solution is octagam 5% liquid is contraindicated in patients who have acute severe hypersensitivity reactions to human immunoglobulin. This formulation utilizes a solution delivery system. Marketed by Octapharma Usa Inc, this product is identified by NDC 68982-840 and is authorized under FDA application BLA125062.

Identification & Billing

NDC Package Code
68982-840-01
Package Description
20 mL in 1 BOTTLE, GLASS
Product Code
11-Digit Billing Format
68982084001
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
Units Per Package
20 ML
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Octagam Immune Globulin (human)
Non-Proprietary Name
Immune Globulin
Substance Name
Human Immunoglobulin G
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)
Usage Information
Octagam 5% liquid is contraindicated in patients who have acute severe hypersensitivity reactions to human immunoglobulin. Octagam 5% liquid contains trace amounts of IgA (not more than 0.2 mg/ml in a 5% solution). It is contraindicated in IgA deficient patients with antibodies against IgA and history of hypersensitivity (See Description [ 11 ]). Octagam 5% liquid is contraindicated in patients with acute hypersensitivity reaction to corn. Octagam 5% liquid contains maltose, a disaccharide sugar which is derived from corn. Patients known to have corn allergies should avoid using Octagam 5% liquid.

Regulatory & Marketing

Labeler Name
Octapharma Usa Inc
Product Type
Plasma Derivative
FDA Application #
BLA125062
Marketing Category
BLA - A product marketed under an approved Biologic License Application.
Start Marketing Date
05-21-2004
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.

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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.

Source: PDAC
INJECTION, IMMUNE GLOBULIN, (OCTAGAM), INTRAVENOUS, NON-LYOPHILIZED (E.G. LIQUID), 500 MG
HCPCS Dosage 500 MG
Units / Pkg

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.

* 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 (68982-840). Click a package code to view its specific billing and regulatory data.

50 mL in 1 BOTTLE, GLASS
100 mL in 1 BOTTLE, GLASS
200 mL in 1 BOTTLE, GLASS
500 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 68982-840-01 identifies a specific commercial package of 20 ml in 1 bottle, glass of Octagam Immune Globulin (human), a plasma derivative labeled by Octapharma Usa Inc. This product is billed per "ML" milliliter and contains an estimated amount of 20 billable units per package. This solution is formulated for intravenous use and contains human immunoglobulin g 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 May 21, 2004. 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: 68982084001. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. There are 20 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:

10-Digit Format (5-3-2)
68982-840-01
11-Digit CMS (5-4-2)
68982-0840-01

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