Dermatitis

• FDA approval · 2008-03-31
  FDA Approved: HYDROXYZINE HYDROCHLORIDE — Original Application (Northstar RxLLC)

  FDA approved Northstar RxLLC's Original Application for hydroxyzine hydrochloride, a generic antihistamine product.

• FDA approval · 2008-03-25
  FDA Approved: CORDRAN — Supplemental Application (INA Pharmaceutics, Inc)

  The FDA approved a supplemental application for Cordran (flurandrenolide) from INA Pharmaceutics, Inc.

• FDA approval · 2007-09-04
  FDA Approved: NYSTATIN AND TRIAMCINOLONE ACETONIDE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)

  The FDA approved a supplemental application for a generic topical product combining nystatin and triamcinolone acetonide (Sun Pharmaceutical…

• FDA approval · 2007-05-21
  FDA Approved: BETAMETHASONE DIPROPIONATE — Original Application (E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC)

  FDA approved the original application for Betamethasone Dipropionate (a generic topical corticosteroid) from E. Fougera & Co., marking appro…

• FDA approval · 2007-05-21
  FDA Approved: BETAMETHASONE DIPROPIONATE — Original Application (Sun Pharmaceutical Industries, Inc.)

  FDA approved a generic topical corticosteroid, Betamethasone Dipropionate, under Sun Pharmaceutical Industries' Original Application.

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• FDA approval · 2006-08-28
  FDA Approved: DIPROLENE — Supplemental Application (Organon LLC)

  FDA approved a supplemental application for Diprolene (betamethasone dipropionate) submitted by Organon LLC, resulting in updated labeling f…

• FDA approval · 2006-08-14
  FDA Approved: CLOBETASOL PROPIONATE — Supplemental Application (E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.)

  FDA approves a supplemental application for clobetasol propionate from E. Fougera & Co. (division of Fougera Pharmaceuticals Inc.), under th…