Cyklx Solution/ Drops
NDC Package 87047-7852-2

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Cyklx (articaine hydrochloride) solution/ dropses is cYKLX is indicated for ocular surface anesthesia prior to ocular procedures and/or intraocular injections in adults and pediatric patients. This formulation utilizes a solution/ drops delivery system. Marketed by American Genomics, Llc, this product is identified by NDC 87047-7852 and is authorized under FDA application NDA218643.

Identification & Billing

NDC Package Code
87047-7852-2
Package Description
2 POUCH in 1 CARTON / 5 VIAL, SINGLE-DOSE in 1 POUCH / .4 mL in 1 VIAL, SINGLE-DOSE
Product Code
87047-7852
11-Digit Billing Format
87047785202
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Cyklx
Non-Proprietary Name
Articaine Hydrochloride
Substance Name
Articaine Hydrochloride
Dosage Form
Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
Administration Route
Ophthalmic - Administration to the external eye.
Active Ingredient(s)
ARTICAINE HYDROCHLORIDE 80 mg/mL
Pharmacologic Class
Usage Information
CYKLX is indicated for ocular surface anesthesia prior to ocular procedures and/or intraocular injections in adults and pediatric patients.

Regulatory & Marketing

Labeler Name
American Genomics, Llc
Product Type
Human Prescription Drug
FDA Application #
NDA218643
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
04-02-2026
Listing Expiration
12-31-2026
Exclude Flag
N
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (87047-7852). Click a package code to view its specific billing and regulatory data.

87047-7852-1
10 POUCH in 1 CARTON / 5 VIAL, SINGLE-DOSE in 1 POUCH / .4 mL in 1 VIAL, SINGLE-DOSE

* 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 87047-7852-2 identifies a specific commercial package of 2 pouch in 1 carton / 5 vial, single-dose in 1 pouch / .4 ml in 1 vial, single-dose of Cyklx, a human prescription drug labeled by American Genomics, Llc. This solution/ drops is formulated for ophthalmic use and contains articaine hydrochloride 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 American Genomics, Llc on April 02, 2026. The current certification is valid through December 31, 2026.

How is this American Genomics, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87047785202. 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)
87047-7852-2
11-Digit CMS (5-4-2)
87047-7852-02

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