Airsupra Aerosol, Metered
NDC Package 0310-9080-28

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

Package Information

Airsupra (albuterol sulfate and budesonide) aerosols is aIRSUPRA is indicated for the as-needed treatment or prevention of bronchoconstriction and to reduce the risk of exacerbations in patients with asthma 18 years of age and older. This formulation utilizes a aerosol, metered delivery system. Marketed by Astrazeneca Pharmaceuticals Lp, this product is identified by NDC 0310-9080 and is authorized under FDA application NDA214070.

Identification & Billing

NDC Package Code
0310-9080-28
Package Description
1 INHALER in 1 CARTON / 28 AEROSOL, METERED in 1 INHALER
Product Code
11-Digit Billing Format
00310908028
Billing Unit
GM - Billing unit of "gram" is used when a product is measured by its weight.
RxNorm Crosswalk
  • RxCUI: 2665906 - albuterol 90 MCG/INHAL / budesonide 80 MCG/INHAL Metered Dose Inhaler, 120 Actuations
  • RxCUI: 2665906 - 120 ACTUAT albuterol 0.09 MG/ACTUAT / budesonide 0.08 MG/ACTUAT Metered Dose Inhaler
  • RxCUI: 2665906 - albuterol sulfate 108 MCG/INHAL / budesonide 80 MCG/INHAL Metered Dose Inhaler, 120 Actuations
  • RxCUI: 2665912 - AIRSUPRA 90/80 MCG/INHAL Metered Dose Inhaler, 120 Actuations
  • RxCUI: 2665912 - 120 ACTUAT albuterol 0.09 MG/ACTUAT / budesonide 0.08 MG/ACTUAT Metered Dose Inhaler [Airsupra]

Clinical Specifications

Proprietary Name
Airsupra
Non-Proprietary Name
Albuterol Sulfate And Budesonide
Substance Name
Albuterol Sulfate; Budesonide
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.
Usage Information
AIRSUPRA is indicated for the as-needed treatment or prevention of bronchoconstriction and to reduce the risk of exacerbations in patients with asthma 18 years of age and older.

Regulatory & Marketing

Labeler Name
Astrazeneca Pharmaceuticals Lp
Product Type
Human Prescription Drug
FDA Application #
NDA214070
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
10-02-2023
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
Yes

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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (0310-9080). Click a package code to view its specific billing and regulatory data.

1 INHALER in 1 CARTON / 120 AEROSOL, METERED in 1 INHALER

* 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 0310-9080-28 identifies a specific commercial package of 1 inhaler in 1 carton / 28 aerosol, metered in 1 inhaler of Airsupra, a human prescription drug labeled by Astrazeneca Pharmaceuticals Lp. This aerosol, metered is formulated for respiratory (inhalation) use and contains albuterol sulfate; budesonide 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 Astrazeneca Pharmaceuticals Lp on October 02, 2023. The current certification is valid through December 31, 2026.

How is this Astrazeneca Pharmaceuticals Lp product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00310908028. Quantities are measured in per "gm or gram", products billed per gram are products measured by weight.. 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 (4-4-2)
0310-9080-28
11-Digit CMS (5-4-2)
00310-9080-28

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