71699-025 : Xcopri 25 mg Oral Tablet, Film Coated


NDC: 71699-025
Labeler: Sk Life Science, Inc.
Product Type: Human Prescription Drug
Drug Name:  Xcopri
Dosage Form: Oral Tablet, Film Coated
Application #: NDA212839
Rev. Date: 
CSA Schedule: CV (US) [1]


[1] Schedule V Controlled Substance: Low potential for abuse relative to substances listed in Schedule IV and consist primarily of preparations containing limited quantities of certain narcotics. (i.e. Cough preparations containing not more than 200 milligrams of Codeine per 100 milliliters or per 100 grams [such as Robitussin AC, Phenergan with Codeine], and Ezogabine). More Details: US Dept of Justice Controlled Substance Schedules.

NDC Package Codes:

  • 71699-025-30: 30 TABLET, FILM COATED IN 1 BOTTLE (71699‑025‑30)

Active Ingredients:

  • Cenobamate

Dosage Strength:

  • 25 mg

Pharmaceutical Classes:

  • Cytochrome P450 2B6 Inducers [MoA]
  • Cytochrome P450 2B6 Inhibitors [MoA]
  • Cytochrome P450 2C19 Inhibitors [MoA]
  • Cytochrome P450 2C8 Inducers [MoA]
  • Cytochrome P450 3A Inhibitors [MoA]
  • Cytochrome P450 3A4 Inducers [MoA]
  • GABA A Receptor Positive Modulators [MoA]
  • Sodium Channel Antagonists [MoA]

Related Products:

Based on records with the same trade name.
  • 71699-050 Xcopri 50 mg Oral Tablet, Film Coated by Sk Life Science, Inc.
  • 71699-100 Xcopri 100 mg Oral Tablet, Film Coated by Sk Life Science, Inc.
  • 71699-150 Xcopri 150 mg Oral Tablet, Film Coated by Sk Life Science, Inc.
  • 71699-200 Xcopri 200 mg Oral Tablet, Film Coated by Sk Life Science, Inc.

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.