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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 021026
Company: MYLAN
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
VUSION MICONAZOLE NITRATE; WHITE PETROLATUM; ZINC OXIDE 0.25%;81.35%;15% OINTMENT;TOPICAL Prescription None Yes Yes
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
02/16/2006 ORIG-1 Approval Type 3 - New Dosage Form STANDARD Label (PDF)
Letter (PDF)
Review
https://www.accessdata.fda.gov/drugsatfda_docs/label/2006/021026s000lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2006/021026ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2006/021026_vusion_toc.cfm
Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
08/29/2018 SUPPL-13 Labeling-Package Insert Label (PDF)
https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/021026s013lbl.pdf
06/16/2016 SUPPL-12 Manufacturing (CMC)

Label is not available on this site.

05/21/2014 SUPPL-11 Manufacturing (CMC)

Label is not available on this site.

04/01/2010 SUPPL-6 Labeling Label (PDF)
Letter (PDF)
https://www.accessdata.fda.gov/drugsatfda_docs/label/2010/021026s006lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2010/021026s006ltr.pdf
10/03/2007 SUPPL-4 Labeling Label (PDF)
Letter (PDF)
https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/021026s004lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2007/021026s004ltr.pdf
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels,
Patient Package Insert
Note Url
08/29/2018 SUPPL-13 Labeling-Package Insert Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/021026s013lbl.pdf
04/01/2010 SUPPL-6 Labeling Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2010/021026s006lbl.pdf
10/03/2007 SUPPL-4 Labeling Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/021026s004lbl.pdf
02/16/2006 ORIG-1 Approval Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2006/021026s000lbl.pdf
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