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`DEPARTMENT OF HEALTH AND HUMAN SERVICES
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` NDA 21976/S-30
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` NDA 202895/S-7
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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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` Janssen Products L.P.
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` Attention: Karen Gerry, BSc
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` Manager, Global Regulatory Affairs
` 1125 Trenton-Harbourton Road
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` Titusville, NJ 08560
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`Dear Ms. Gerry:
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`Please refer to your Supplemental New Drug Applications (sNDA) dated and received August
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`24, 2012 submitted under section 505(b) of the Federal Food, Drug, and Cosmetic Act (FDCA)
` for Prezista® (darunavir) tablets, 75 mg, 150 mg, 400 mg, 600 mg, and 800 mg, and Prezista®
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` (darunavir) oral suspension, 100 mg/mL.
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` We acknowledge receipt of your amendments dated November 28, 2012, January 15, 2013, and
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` February 15, 2013.
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` These Prior Approval supplemental new drug applications propose to update labeling (package
` insert and patient package insert) with information from a drug-drug interaction trial of Prezista®
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`(darunavir) in combination with the antimalarial drug Coartem® (artemether/lumefantrine).
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`We have completed our review of these supplemental applications, as amended. They are
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`approved, effective on the date of this letter, for use as recommended in the enclosed, agreed-
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`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, patient package
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`insert, and Instructions for Use), with the addition of any labeling changes in pending “Changes
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`Being Effected” (CBE) supplements, as well as annual reportable changes not included in the
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`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: 3265710
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` NDA 21976/S-30
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` NDA 202895/S-7
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` Page 2
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`http://www.fda.gov/downloads/DrugsGuidanceComplianceRegulatoryInformation/Guidances/U
`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
`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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`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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`If you have any questions, call Linda C. Onaga, Regulatory Project Manager, at (301) 796-0759
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`or (301) 796-1500.
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`Sincerely,
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`{See appended electronic signature page}
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`Debra Birnkrant, MD
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`Director
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`Division of Antiviral Products
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`Office of Antimicrobial Products
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`Center for Drug Evaluation and Research
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`ENCLOSURE(S):
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`Content of Labeling
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`Reference ID: 3265710
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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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`KENDALL A MARCUS
`02/22/2013
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`Reference ID: 3265710
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