Trimbow Aerosol, Metered
NDC Package 10122-121-02

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

Package Information

Trimbow (beclomethasone dipropionate/formoterol fumarate/glycopyrrolate) aerosols is tRIMBOW is indicated for the maintenance treatment of asthma in adult patients aged 18 years and older. This formulation utilizes a aerosol, metered delivery system. Marketed by Chiesi Usa, Inc., this product is identified by NDC 10122-121 and is authorized under FDA application NDA219622.

Identification & Billing

NDC Package Code
10122-121-02
Package Description
1 CANISTER in 1 CARTON / 120 AEROSOL, METERED in 1 CANISTER
Product Code
10122-121
11-Digit Billing Format
10122012102

Clinical Specifications

Proprietary Name
Trimbow
Non-Proprietary Name
Beclomethasone Dipropionate/formoterol Fumarate/glycopyrrolate
Substance Name
Beclomethasone Dipropionate; Formoterol Fumarate; Glycopyrrolate
Dosage Form
Aerosol, Metered - A pressurized dosage form consisting of metered dose valves which allow for the delivery of a uniform quantity of spray upon each activation.
Administration Route
Respiratory (inhalation) - Administration within the respiratory tract by inhaling orally or nasally for local or systemic effect.
Active Ingredient(s)
Pharmacologic Class
Usage Information
TRIMBOW is indicated for the maintenance treatment of asthma in adult patients aged 18 years and older. Limitations of UseTRIMBOW is NOT indicated for relief of acute bronchospasm [see Warnings and Precautions (5.2)].

Regulatory & Marketing

Labeler Name
Chiesi Usa, Inc.
Product Type
Human Prescription Drug
FDA Application #
NDA219622
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
05-14-2026
Listing Expiration
12-31-2027
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.

* 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 10122-121-02 identifies a specific commercial package of 1 canister in 1 carton / 120 aerosol, metered in 1 canister of Trimbow, a human prescription drug labeled by Chiesi Usa, Inc.. This aerosol, metered is formulated for respiratory (inhalation) use and contains beclomethasone dipropionate; formoterol fumarate; glycopyrrolate 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 Chiesi Usa, Inc. on May 14, 2026. The current certification is valid through December 31, 2027.

How is this Chiesi Usa, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 10122012102. 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)
10122-121-02
11-Digit CMS (5-4-2)
10122-0121-02

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