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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 213690
Company: JOURNEY
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
ZILXI MINOCYCLINE HYDROCHLORIDE EQ 1.5% BASE AEROSOL, FOAM;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
05/28/2020 ORIG-1 Approval Type 5 - New Formulation or New Manufacturer STANDARD Label (PDF)
Letter (PDF)
Review
https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/213690s000lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2020/213690Orig1s000ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2020/213690Orig1s000TOC.cfm
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels,
Patient Package Insert
Note Url
05/28/2020 ORIG-1 Approval Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/213690s000lbl.pdf
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