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Data / Drug companies / SK Life Science, Inc.

SK Life Science, Inc.: 11 products in the FDA NDC directory, labeler code 71699

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

SK Life Science, Inc. (labeler code 71699) lists 11 products in the FDA National Drug Code Directory, covering 1 finished drug by generic name. By type: 11 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on August 29, 2025.

The request: Watch SK Life Science, Inc. (FDA labeler code 71699): each new product listing and each discontinued product. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
71699
Products in commercial distribution
11
Packages
12
Finished drugs by generic name
1
Prescription products
11
Over the counter products
0
Controlled substance products
Schedule V 6
Flagged as original packager
11 of 11 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
March 12, 2020
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
New drug applications (NDA)11100%

Products by type

TypeProductsShare
Prescription drugs11100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

DrugProductsCompanies listing it
Cenobamate111

Dosage forms

Dosage formProductsShare
Tablet, film coated545.5%
Kit545.5%
Tablet19.1%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Xcopri71699-204TabletNew drug applications (NDA)August 29, 2025
Xcopri71699-025Tablet, film coatedNew drug applications (NDA)April 6, 2024
Xcopri Maintenance Pack71699-104KitNew drug applications (NDA)April 30, 2021
Xcopri71699-050Tablet, film coatedNew drug applications (NDA)April 30, 2021
Xcopri Titration Pack71699-203KitNew drug applications (NDA)March 12, 2020
Xcopri Titration Pack71699-202KitNew drug applications (NDA)March 12, 2020
Xcopri Titration Pack71699-201KitNew drug applications (NDA)March 12, 2020
Xcopri71699-200Tablet, film coatedNew drug applications (NDA)March 12, 2020
Xcopri71699-150Tablet, film coatedNew drug applications (NDA)March 12, 2020
Xcopri Maintenance Pack71699-103KitNew drug applications (NDA)March 12, 2020
Xcopri71699-100Tablet, film coatedNew drug applications (NDA)March 12, 2020

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.