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• FDA approval · 2018-04-23
  FDA Approved: FLUOCINONIDE — Original Application (NorthStar RxLLC)

  FDA approved Fluocinonide through an Original Application (generic) submitted by NorthStar RxLLC.

• FDA approval · 2018-04-17
  FDA Approved: CLOBETASOL PROPIONATE — Original Application (Xiromed, LLC)

  FDA approved the original application for clobetasol propionate (topical) by Xiromed, LLC. It is a potent corticosteroid indicated for corti…

• FDA approval · 2018-03-28
  FDA Approved: DIPROLENE — Supplemental Application (Organon LLC)

  FDA approved a supplemental application for Diprolene (betamethasone dipropionate) from Organon LLC.

• FDA approval · 2018-02-13
  FDA Approved: BETAMETHASONE DIPROPIONATE — Original Application (Encube Ethicals, Inc.)

  FDA approved Betamethasone Dipropionate as an original application from Encube Ethicals, Inc. (ANDA206389) for topical use in inflammatory d…

• FDA approval · 2017-11-21
  FDA Approved: HYDROCORTISONE BUTYRATE — Original Application (The J. Molner Company LLC)

  The FDA approved a generic topical hydrocortisone butyrate product under an Original Application (ANDA 209556) from The J. Molner Company LL…

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• FDA approval · 2017-10-27
  FDA Approved: CLOBETASOL PROPIONATE — Original Application (Zydus Pharmaceuticals USA Inc.)

  FDA approved the original ANDA for a generic clobetasol propionate topical product from Zydus Pharmaceuticals USA Inc.

• FDA approval · 2017-10-25
  FDA Approved: CLOBETASOL PROPIONATE — Original Application (Macleods Pharmaceuticals Limited)

  FDA approved the original abbreviated new drug application for clobetasol propionate from Macleods Pharmaceuticals Limited.

• FDA approval · 2017-09-22
  FDA Approved: CLOBETASOL PROPIONATE — Original Application (Lupin Pharmaceuticals, Inc.)

  FDA approved Lupin Pharmaceuticals' original application for clobetasol propionate as a generic topical corticosteroid.

• FDA approval · 2017-03-20
  FDA Approved: CLOBETASOL PROPIONATE — Original Application (Northstar Rx LLC)

  FDA approved the original application for a generic clobetasol propionate topical corticosteroid, manufactured by Northstar Rx LLC. The appr…

• FDA approval · 2017-01-11
  FDA Approved: DESOXIMETASONE — Original Application (Lupin Pharmaceuticals, Inc.)

  FDA approved Lupin Pharmaceuticals' desoximetasone topical generic under an Original Application (ANDA 208163).

• FDA approval · 2016-12-13
  FDA Approved: DERMOTIC — Supplemental Application (Royal Pharmaceuticals)

  The FDA approved a supplemental application for DERMOTIC (fluocinonide acetate) from Royal Pharmaceuticals.

• FDA approval · 2016-10-26
  FDA Approved: TRIAMCINOLONE ACETONIDE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)

  FDA granted approval of a supplemental application for Triamcinolone Acetonide submitted by Sun Pharmaceutical Industries, Inc., resulting i…

• FDA approval · 2016-05-19
  FDA Approved: FLUOCINOLONE ACETONIDE — Original Application (Sun Pharmaceutical Industries, Inc.)

  FDA approved Sun Pharmaceutical Industries' fluocinonide acetonide topical product through an original generic application (ANDA).

• FDA approval · 2016-05-12
  FDA Approved: BETAMETHASONE DIPROPIONATE — Supplemental Application (E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC)

  The FDA approved a supplemental application for Betamethasone Dipropionate from E. Fougera & Co., authorizing changes to the approved produc…

• FDA approval · 2016-05-10
  FDA Approved: DESOXIMETASONE — Original Application (Novel Laboratories, Inc.)

  FDA approves a generic topical desoximetasone from Novel Laboratories, Inc. under an Original Application (ANDA 206792).

• FDA approval · 2016-04-25
  FDA Approved: FLUOCINOLONE ACETONIDE OIL — Original Application (Rising Pharma Holdings, Inc.)

  FDA approves Rising Pharma Holdings' Fluocinonide Acetonide Oil as a generic topical corticosteroid for inflammatory and pruritic skin condi…

• FDA approval · 2015-01-20
  FDA Approved: BETAMETHASONE VALERATE — Supplemental Application (E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC)

  The FDA approved a supplemental application for Betamethasone valerate from E. Fougera & Co., a division of Fougera Pharmaceuticals, LLC. Th…

• FDA approval · 2014-07-18
  FDA Approved: DESOXIMETASONE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)

  The FDA approved a supplemental application for Desoximetasone from Sun Pharmaceutical Industries, updating or expanding its labeling.

• FDA approval · 2014-07-14
  FDA Approved: FLUOCINONIDE — Original Application (Glenmark Pharmaceuticals Inc., USA)

  The FDA approved Glenmark's Original Application for fluocinonide, a topical corticosteroid, as a generic product. This marks regulatory cle…

• FDA approval · 2014-07-14
  FDA Approved: FLUOCINONIDE — Original Application (Sun Pharmaceutical Industries, Inc.)

  FDA approved an original application for fluocinonide from Sun Pharmaceutical Industries, a topical corticosteroid. The product is indicated…

• FDA approval · 2014-05-15
  FDA Approved: TRIDESILON CREAM — Supplemental Application (Encore Dermatology Inc)

  FDA approved a supplemental application for TRIDESILON CREAM (desonide 0.05%), indicating a regulatory action related to this dermatology pr…

• FDA approval · 2014-05-12
  FDA Approved: DESOXIMETASONE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)

  The FDA has approved a supplemental application for Desoximetasone from Sun Pharmaceutical Industries, Inc.

• FDA approval · 2013-08-09
  FDA Approved: FLUOCINOLONE ACETONIDE — Original Application (Padagis Israel Pharmaceuticals Ltd)

  FDA approved an original application for a generic fluocinonide acetonide topical product by Padagis Israel Pharmaceuticals Ltd.

• FDA approval · 2013-07-23
  FDA Approved: CORDRAN — Supplemental Application (INA Pharmaceutics, Inc)

  FDA approved a supplemental application for Cordran (Flurandrenolide) submitted by INA Pharmaceutics, Inc. The update pertains to changes to…

• FDA approval · 2012-08-17
  FDA Approved: CLOBEX — Supplemental Application (Galderma Laboratories, L.P.)

  The FDA approved a supplemental application for CLOBEX (clobetasol propionate) submitted by Galderma Laboratories to update its labeling.