Flector System
NDC Package 71858-0405-2
Package Information
Flector (diclofenac epolamine) systems is diclofenac patches are used to relieve pain from various conditions (e.g., sprained ankle). This formulation utilizes a system delivery system. Marketed by Ibsa Pharma Inc., this product is identified by NDC 71858-0405 and is authorized under FDA application NDA021234.
Identification & Billing
- RxCUI: 855626 - diclofenac epolamine 1.3 % Twice-Daily Medicated Patch
- RxCUI: 855626 - Twice-Daily diclofenac epolamine 0.013 MG/MG Medicated Patch
- RxCUI: 855628 - Flector 1.3 % Twice-Daily Medicated Patch
- RxCUI: 855628 - Twice-Daily diclofenac epolamine 0.013 MG/MG Medicated Patch [Flector]
- RxCUI: 855628 - Twice-Daily Flector 0.013 MG/MG Medicated Patch
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 71858 - Ibsa Pharma Inc.
- 71858-0405 - Flector
- 71858-0405-2 - 1 POUCH in 1 CARTON / 2 SYSTEM in 1 POUCH (71858-0405-1)
- 71858-0405 - Flector
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 (71858-0405). 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 71858-0405-2 identifies a specific commercial package of 1 pouch in 1 carton / 2 system in 1 pouch (71858-0405-1) of Flector, a human prescription drug labeled by Ibsa Pharma Inc.. This system is formulated for topical use and contains diclofenac epolamine 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 Ibsa Pharma Inc. on November 01, 2020. The current certification is valid through December 31, 2026.
What are the primary indications for this medication?
Diclofenac patches are used to relieve pain from various conditions (e.g., sprained ankle). This medication is known as a nonsteroidal anti-inflammatory drug (NSAID). If you are treating a chronic condition such as arthritis, ask your doctor about non-drug treatments and/or using other medications to treat your pain. See also Warning section.
How is this Ibsa Pharma Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 71858040502. 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 Package segment to maintain the 5-4-2 structure.