Yupelri Solution
NDC Package 49502-806-87
Package Information
Yupelri (revefenacin) solution is revefenacin is a long-term medication used to treat an ongoing lung disease, chronic obstructive pulmonary disease (COPD). This formulation utilizes a solution delivery system. Marketed by Viatris Specialty Llc, this product is identified by NDC 49502-806 and is authorized under FDA application NDA210598.
Identification & Billing
- RxCUI: 2102779 - revefenacin 175 MCG in 3 ML Inhalation Solution
- RxCUI: 2102779 - revefenacin 0.0583 MG/ML Inhalation Solution
- RxCUI: 2102779 - revefenacin 175 MCG per 3 ML Inhalation Solution
- RxCUI: 2102784 - YUPELRI 175 MCG in 3 ML Inhalation Solution
- RxCUI: 2102784 - revefenacin 0.0583 MG/ML Inhalation Solution [Yupelri]
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 49502 - Viatris Specialty Llc
- 49502-806 - Yupelri
- 49502-806-87 - 7 POUCH in 1 CARTON / 1 VIAL, SINGLE-DOSE in 1 POUCH (49502-806-33) / 3 mL in 1 VIAL, SINGLE-DOSE
- 49502-806 - Yupelri
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 (49502-806). Click a package code to view its specific billing and regulatory data.
* 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 49502-806-87 identifies a specific commercial package of 7 pouch in 1 carton / 1 vial, single-dose in 1 pouch (49502-806-33) / 3 ml in 1 vial, single-dose of Yupelri, a human prescription drug labeled by Viatris Specialty Llc. This solution is formulated for respiratory (inhalation) use and contains revefenacin 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 Viatris Specialty Llc on December 03, 2018. The current certification is valid through December 31, 2026.
What are the primary indications for this medication?
Revefenacin is a long-term medication used to treat an ongoing lung disease, chronic obstructive pulmonary disease (COPD). It must be used regularly to reduce and prevent symptoms such as shortness of breath, cough, and wheezing. This medication belongs to a class of drugs known as anticholinergics. It works by relaxing the muscles around the airways so that they open up and you can breathe more easily. Revefenacin does not work right away and should not be used to relieve sudden breathing problems. If wheezing or sudden shortness of breath occurs, use your quick-relief inhaler as prescribed.
How is this Viatris Specialty Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 49502080687. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.