Bedinvetmab Solution
NDC Package 54771-2782-1

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

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.

Bedinvetmab solution is a bulk ingredient utilized for pharmaceutical compounding or manufacturing. This formulation utilizes a solution delivery system. Marketed by Zoetis Inc., this product is identified by NDC 54771-2782.

Identification & Billing

NDC Package Code
54771-2782-1
Package Description
1 kg in 1 BAG
Product Code
11-Digit Billing Format
54771278201

Clinical Specifications

Proprietary Name
Bedinvetmab
Non-Proprietary Name
Bedinvetmab
Substance Name
Bedinvetmab
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)

Regulatory & Marketing

Labeler Name
Zoetis Inc.
Product Type
Bulk Ingredient
Marketing Category
BULK INGREDIENT - A category specifying that a product is marketed as a bulk ingredient.
Start Marketing Date
01-23-2020
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 54771-2782-1 identifies a specific commercial package of 1 kg in 1 bag of Bedinvetmab (UNFINISHED drug), a bulk ingredient labeled by Zoetis Inc.. This solution is formulated for use and contains bedinvetmab 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 Zoetis Inc. on January 23, 2020. The current certification is valid through December 31, 2026.

How is this Zoetis Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 54771278201. 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 (5-4-1)
54771-2782-1
11-Digit CMS (5-4-2)
54771-2782-01

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