Ravicti Liquid
NDC Package 75987-050-06
Package Information
Ravicti (glycerol phenylbutyrate) liquids is a medication used along with diet changes for long-term treatment of a certain inherited disorder (urea cycle disorder). This formulation utilizes a liquid delivery system. Marketed by Horizon Therapeutics Usa, Inc., this product is identified by NDC 75987-050 and is authorized under FDA application NDA203284.
Identification & Billing
- RxCUI: 1368453 - glycerol phenylbutyrate 1.1 GM in 1 mL Oral Solution
- RxCUI: 1368453 - glycerol phenylbutyrate 1100 MG/ML Oral Solution
- RxCUI: 1368453 - glycerol phenylbutyrate 1.1 GM per 1 ML Oral Solution
- RxCUI: 1368459 - RAVICTI 1.1 GM in 1 mL Oral Solution
- RxCUI: 1368459 - glycerol phenylbutyrate 1100 MG/ML Oral Solution [Ravicti]
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 75987 - Horizon Therapeutics Usa, Inc.
- 75987-050 - Ravicti
- 75987-050-06 - 1 BOTTLE in 1 CARTON / 25 mL in 1 BOTTLE
- 75987-050 - Ravicti
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 (75987-050). 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 75987-050-06 identifies a specific commercial package of 1 bottle in 1 carton / 25 ml in 1 bottle of Ravicti, a human prescription drug labeled by Horizon Therapeutics Usa, Inc.. This liquid is formulated for oral use and contains glycerol phenylbutyrate 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 Horizon Therapeutics Usa, Inc. on February 28, 2013. The current certification is valid through December 31, 2026.
What are the primary indications for this medication?
This medication is used along with diet changes for long-term treatment of a certain inherited disorder (urea cycle disorder). It helps remove a certain chemical (ammonia) from the body. Too much ammonia in the body can cause brain damage and sometimes death. This medication should not be used to treat sudden, severely high levels of ammonia in the body. Get medical help right away if you have sudden symptoms of too much ammonia, such as trouble thinking, vomiting, irritability, trouble speaking, trouble walking, fainting.
How is this Horizon Therapeutics Usa, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 75987005006. 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.