Ventolin
NDC Package 50436-6050-0

11-digit billing NDC: 50436605000 · Billing unit: GM
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Ventolin is hFA is contraindicated in patients with a history of hypersensitivity to albuterol or any other components of VENTOLIN HFA. Marketed by Unit Dose Services, this product is identified by NDC 50436-6050 and is authorized under FDA application NDA020983.

Identification & Billing

NDC Package Code
50436-6050-0
Package Description
90 AEROSOL, METERED in 1 BOTTLE
Product Code
50436-6050
11-Digit Billing Format
50436605000
Billing Unit
GM - Billing unit of "gram" is used when a product is measured by its weight.
RxNorm Crosswalk
  • RxCUI: 2123076 - albuterol 90 MCG/INHAL Metered Dose Inhaler, 200 Actuation, generic for Ventolin
  • RxCUI: 2123076 - NDA020983 200 ACTUAT albuterol 0.09 MG/ACTUAT Metered Dose Inhaler
  • RxCUI: 859088 - Ventolin HFA 90 MCG/INHAL Metered Dose Inhaler, 200 Actuations
  • RxCUI: 859088 - NDA020983 200 ACTUAT albuterol 0.09 MG/ACTUAT Metered Dose Inhaler [Ventolin]
  • RxCUI: 859088 - NDA020983 200 ACTUAT Ventolin 0.09 MG/ACTUAT Metered Dose Inhaler

Clinical Specifications

Proprietary Name
Ventolin Hfa
Dosage Form
-
Usage Information
VENTOLIN HFA is contraindicated in patients with a history of hypersensitivity to albuterol or any other components of VENTOLIN HFA. Rare cases of hypersensitivity reactions, including urticaria, angioedema, and rash have been reported after the use of albuterol sulfate.

Regulatory & Marketing

Labeler Name
Unit Dose Services
FDA Application #
NDA020983
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
06-09-2006
Listing Expiration
12-31-2019
Exclude Flag
I
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 50436-6050-0 identifies a specific commercial package of 90 aerosol, metered in 1 bottle of Ventolin Hfa, labeled by Unit Dose Services. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Unit Dose Services on June 09, 2006. The current certification is valid through December 31, 2019.

How is this Unit Dose Services product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50436605000. 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 (5-4-1)
50436-6050-0
11-Digit CMS (5-4-2)
50436-6050-00

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