Androgenetic Alopecia

• FDA label_change · 2024-08-22
  FDA Approved: FINASTERIDE — Supplemental Application (Accord Healthcare, Inc.)

  FDA approves a supplemental application for finasteride from Accord Healthcare, Inc., resulting in labeling changes.

• FDA label_change · 2015-04-27
  FDA Approved: WOMENS ROGAINE UNSCENTED — Supplemental Application (Kenvue Brands LLC)

  FDA approved a supplemental application for Women's Rogaine Unscented (minoxidil) filed by Kenvue Brands LLC, authorizing labeling changes f…

• FDA label_change · 2014-12-15
  FDA Approved: FINASTERIDE — Supplemental Application (Accord Healthcare, Inc.)

  FDA approved a supplemental application for Finasteride by Accord Healthcare, Inc., updating the drug's labeling. The supplement likely incl…

• FDA label_change · 2014-11-28
  FDA Approved: MINOXIDIL — Supplemental Application (Endo USA, Inc.)

  FDA approved a supplemental application for MINOXIDIL from Endo USA, Inc., updating the labeling for the treatment of androgenetic alopecia.

• FDA label_change · 2012-12-29
  FDA Approved: FINASTERIDE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)

  The FDA approved a supplemental application for finasteride submitted by Teva Pharmaceuticals USA, Inc.

• Want full summaries, importance scores, and drug timelines? Upgrade to Plus or Pro.
• FDA label_change · 2011-06-09
  FDA Approved: PROPECIA — Supplemental Application (Organon LLC)

  The FDA approved a supplemental application for PROPECIA (finasteride) from Organon LLC, updating the labeling for the product.

• FDA label_change · 2011-03-11
  FDA Approved: PROPECIA — Supplemental Application (Organon LLC)

  The FDA approved a supplemental labeling change for Propecia (finasteride) submitted by Organon LLC.

• FDA label_change · 2010-03-24
  FDA Approved: PROPECIA — Supplemental Application (Organon LLC)

  The FDA approved a supplemental application for PROPECIA (finasteride) submitted by Organon LLC, resulting in changes to the product labelin…

• FDA label_change · 2006-09-12
  FDA Approved: MENS ROGAINE EXTRA STRENGTH UNSCENTED — Supplemental Application (Kenvue Brands LLC)

  The FDA approved a supplemental application to add the Men’s Rogaine Extra Strength Unscented minoxidil product (5% topical solution) by Ken…

• FDA label_change · 2006-05-22
  FDA Approved: WOMENS ROGAINE UNSCENTED — Supplemental Application (Kenvue Brands LLC)

  FDA approved a supplemental application for Women's Rogaine Unscented (minoxidil) from Kenvue Brands LLC, updating the product labeling to r…