Braftovi Capsule
NDC Package 70255-025-01
Package Information
Braftovi (encorafenib) capsules is encorafenib is used to treat certain types of cancer (such as melanoma skin cancer, cancer in the colon or rectum). This formulation utilizes a capsule delivery system. Marketed by Array Biopharma Inc., this product is identified by NDC 70255-025 and is authorized under FDA application NDA210496.
Identification & Billing
- RxCUI: 2049119 - encorafenib 75 MG Oral Capsule
- RxCUI: 2049121 - BRAFTOVI 75 MG Oral Capsule
- RxCUI: 2049121 - encorafenib 75 MG Oral Capsule [Braftovi]
- RxCUI: 2049121 - Braftovi 75 MG Oral Capsule
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 70255 - Array Biopharma Inc.
- 70255-025 - Braftovi
- 70255-025-01 - 2 BOTTLE in 1 CARTON / 90 CAPSULE in 1 BOTTLE (70255-025-02)
- 70255-025 - Braftovi
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 (70255-025). 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 70255-025-01 identifies a specific commercial package of 2 bottle in 1 carton / 90 capsule in 1 bottle (70255-025-02) of Braftovi, a human prescription drug labeled by Array Biopharma Inc.. This product is billed for "EA" each discreet unit and contains an estimated amount of 2 billable units per package. This capsule is formulated for oral use and contains encorafenib 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 Array Biopharma Inc. on June 27, 2018. The current certification is valid through December 31, 2027.
What are the primary indications for this medication?
Encorafenib is used to treat certain types of cancer (such as melanoma skin cancer, cancer in the colon or rectum). Encorafenib belongs to a class of drugs known as kinase inhibitors. It works by slowing or stopping the growth of cancer cells.
How is this Array Biopharma Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 70255002501. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 2 total billable units per package. 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.