Interferon-gamma1b Solution
NDC Package 12714-080-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

Interferon-gamma1b solution is a drug for further processing. This formulation utilizes a solution delivery system. Marketed by Boehringer Ingelheim Pharma Gmbh And Co. Kg, this product is identified by NDC 12714-080.

Identification & Billing

NDC Package Code
12714-080-01
Package Description
.1 mg in 1 VIAL, SINGLE-DOSE
Product Code
12714-080
11-Digit Billing Format
12714008001

Clinical Specifications

Proprietary Name
Interferon-gamma1b
Non-Proprietary Name
Interferon-gamma1b
Substance Name
Interferon Gamma-1b
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.
Active Ingredient(s)
INTERFERON GAMMA-1B .1 mg/.1mg

Regulatory & Marketing

Labeler Name
Boehringer Ingelheim Pharma Gmbh And Co. Kg
Product Type
Drug For Further Processing
Marketing Category
DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
Start Marketing Date
09-17-2001
Listing Expiration
12-31-2026
Exclude Flag
N
Unfinished Product
Yes
Sample Package
N/A

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.

* 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 12714-080-01 identifies a specific commercial package of .1 mg in 1 vial, single-dose of Interferon-gamma1b (UNFINISHED drug), drug for further processing labeled by Boehringer Ingelheim Pharma Gmbh And Co. Kg. This solution is formulated for use and contains interferon gamma-1b 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 Boehringer Ingelheim Pharma Gmbh And Co. Kg on September 17, 2001. The current certification is valid through December 31, 2026.

How is this Boehringer Ingelheim Pharma Gmbh And Co. Kg product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 12714008001. 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)
12714-080-01
11-Digit CMS (5-4-2)
12714-0080-01

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