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`DEPARTMENT OF HEALTH AND HUMAN SERVICES
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` NDA 022253/S-030
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` NDA 022254/S-022
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` NDA 022255/S-016
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`Food and Drug Administration
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` Silver Spring MD 20993
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`SUPPLEMENT APPROVAL
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`UCB, Inc.
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`Attention: Susan Tegtmeyer, M.S.
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`Associate Director, Regulatory Affairs
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`1950 Lake Park Drive,
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`Smyrna, Georgia 30080
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`Dear Ms. Tegtmeyer:
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`Please refer to your Supplemental New Drug Applications (sNDAs) dated June 30, 2014,
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`received June 30, 2014, submitted under section 505(b) of the Federal Food, Drug, and Cosmetic
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`Act (FDCA) for Vimpat (lacosamide) tablets, Vimpat (lacosamide) Injection, and Vimpat
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`(lacosamide) oral solution.
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`We acknowledge receipt of your amendments dated August 25, 2014; September 12, 2014; and
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`February 12, 2015.
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`These “Changes Being Effected” supplemental new drug applications provide for revised
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`labeling to update Section 10.1 to include postmarketing overdose experience and to make minor
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`clarifications to the clinical overdose experience description.
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`APPROVAL & LABELING
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`We have completed our review of these supplemental applications. They are approved, effective
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`on the date of this letter, for use as recommended in the enclosed, agreed-upon labeling text.
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`CONTENT OF LABELING
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`As soon as possible, but no later than 14 days from the date of this letter, submit the content of
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`labeling [21 CFR 314.50(l)] in structured product labeling (SPL) format using the FDA
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`automated drug registration and listing system (eLIST), as described at
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`http://www.fda.gov/ForIndustry/DataStandards/StructuredProductLabeling/default.htm. Content
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`of labeling must be identical to the enclosed labeling (text for the package insert and Medication
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`Guide), with the addition of any labeling changes in pending “Changes Being Effected” (CBE)
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`supplements, as well as annual reportable changes not included in the enclosed labeling.
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`Information on submitting SPL files using eList may be found in the guidance for industry titled
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`“SPL Standard for Content of Labeling Technical Qs and As at
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`Reference ID: 3789692
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` NDA 022253/S-030
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` NDA 022254/S-022
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` NDA 022255/S-016
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` Page 2
`http://www.fda.gov/downloads/DrugsGuidanceComplianceRegulatoryInformation/Guidances/U
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` CM072392.pdf
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`The SPL will be accessible from publicly available labeling repositories.
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`Also within 14 days, amend all pending supplemental applications that includes labeling changes
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`for this NDA, including CBE supplements for which FDA has not yet issued an action letter,
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`with the content of labeling [21 CFR 314.50(l)(1)(i)] in MS Word format, that includes the
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`changes approved in this supplemental application, as well as annual reportable changes and
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`annotate each change. To facilitate review of your submission, provide a highlighted or marked-
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`up copy that shows all changes, as well as a clean Microsoft Word version. The marked-up copy
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`should provide appropriate annotations, including supplement number(s) and annual report
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`date(s).
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`PROMOTIONAL MATERIALS
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`You may request advisory comments on proposed introductory advertising and promotional
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`labeling. To do so, submit the following, in triplicate, (1) a cover letter requesting advisory
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`comments, (2) the proposed materials in draft or mock-up form with annotated references, and
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`(3) the package insert(s) to:
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`Food and Drug Administration
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`Center for Drug Evaluation and Research
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`Office of Prescription Drug Promotion (OPDP)
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`5901-B Ammendale Road
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`Beltsville, MD 20705-1266
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`You must submit final promotional materials and package insert(s), accompanied by a Form
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`FDA 2253, at the time of initial dissemination or publication [21 CFR 314.81(b)(3)(i)]. Form
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`FDA 2253 is available at
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`http://www.fda.gov/downloads/AboutFDA/ReportsManualsForms/Forms/UCM083570.pdf.
`Information and Instructions for completing the form can be found at
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`http://www.fda.gov/downloads/AboutFDA/ReportsManualsForms/Forms/UCM375154.pdf. For
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`more information about submission of promotional materials to the Office of Prescription Drug
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`Promotion (OPDP), see http://www.fda.gov/AboutFDA/CentersOffices/CDER/ucm090142.htm.
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`REPORTING REQUIREMENTS
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`We remind you that you must comply with reporting requirements for an approved NDA
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`(21 CFR 314.80 and 314.81).
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`Reference ID: 3789692
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`Sincerely,
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`{See appended electronic signature page}
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`Billy Dunn, M.D.
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`Director
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`Division of Neurology Products
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`Office of Drug Evaluation I
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`Center for Drug Evaluation and Research
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` NDA 022253/S-030
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` NDA 022254/S-022
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` NDA 022255/S-016
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` Page 3
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` If you have any questions, call Stephanie N. Parncutt, MHA, Regulatory Project Manager, at
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` (301) 796-4098.
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`ENCLOSURE(S):
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`Content of Labeling
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`Reference ID: 3789692
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`---------------------------------------------------------------------------------------------------------
`This is a representation of an electronic record that was signed
`electronically and this page is the manifestation of the electronic
`signature.
`---------------------------------------------------------------------------------------------------------
`/s/
`----------------------------------------------------
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`WILLIAM H Dunn
`07/09/2015
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`Reference ID: 3789692
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