Dermatitis

• FDA approval · 2017-01-09
  FDA Approved: DESOXIMETASONE — Original Application (Lupin Pharmaceuticals, Inc.)

  FDA approved Lupin Pharmaceuticals' desoximetasone as a generic topical corticosteroid under an original ANDA.

• FDA approval · 2017-01-06
  FDA Approved: DESOXIMETASONE — Original Application (Saptalis Pharmaceuticals, LLC.)

  The FDA approved an original ANDA application from Saptalis Pharmaceuticals for a desoximetasone topical product, a generic corticosteroid f…

• FDA approval · 2016-12-20
  FDA Approved: NYSTATIN AND TRIAMCINOLONE ACETONIDE — Original Application (Padagis Israel Pharmaceuticals Ltd)

  FDA approved Padagis Israel Pharmaceuticals Ltd's Nystatin and Triamcinolone Acetonide as an Original Application (ANDA) for a topical antif…

• 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 · 2016-12-12
  FDA Approved: DESOXIMETASONE — Original Application (Lupin Pharmaceuticals, Inc.)

  FDA approved Lupin Pharmaceuticals' generic desoximetasone topical (original application) for relief of inflammatory and pruritic manifestat…

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• FDA approval · 2016-11-07
  FDA Approved: DESOXIMETASONE — Original Application (Actavis Pharma, Inc.)

  FDA approved Actavis Pharma's generic desoximetasone under an original ANDA, enabling a new topical corticosteroid product to reach the mark…

• 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 · 2016-10-21
  FDA Approved: FLUOCINOLONE ACETONIDE TOPICAL — Original Application (Actavis Pharma, Inc.)

  FDA approved a generic fluocinonide acetonide topical product under an original application from Actavis Pharma, Inc.

• FDA approval · 2016-08-05
  FDA Approved: TRIAMCINOLONE ACETONIDE — Original Application (Glenmark Pharmaceuticals Inc., USA)

  FDA approved the Original Application (ANDA) for Triamcinolone Acetonide, a generic product manufactured by Glenmark Pharmaceuticals Inc., U…

• FDA approval · 2016-07-28
  FDA Approved: PSORCON — Supplemental Application (Sun Pharmaceutical Industries, Inc.)

  FDA approved a supplemental application for PSORCON (diflorasone diacetate) filed by Sun Pharmaceutical Industries, likely updating labeling…

• FDA approval · 2016-07-22
  FDA Approved: TRIAMCINOLONE ACETONIDE — Original Application (Glenmark Pharmaceuticals Inc., USA)

  FDA approves Glenmark's generic Triamcinolone Acetonide under Original Application (ANDA 206379) for topical corticosteroid use in inflammat…

• FDA approval · 2016-06-23
  FDA Approved: NYSTATIN AND TRIAMCINOLONE ACETONIDE — Original Application (Glenmark Pharmaceuticals Inc., USA)

  FDA approved Glenmark's generic Nystatin and Triamcinolone Acetonide topical ointment (ANDA 208300) for the treatment of cutaneous candidias…

• FDA approval · 2016-06-08
  FDA Approved: DESONIDE — Supplemental Application (Padagis Israel Pharmaceuticals Ltd)

  The FDA approved a supplemental application for DESONIDE submitted by Padagis Israel Pharmaceuticals Ltd, resulting in labeling changes for …

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

  FDA approved Sun Pharmaceutical Industries' fluocinonide acetonide topical product as an original application (ANDA 202368). The generic top…

• 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 · 2015-11-23
  FDA Approved: CLOBETASOL PROPIONATE — Original Application (Lupin Pharmaceuticals,Inc.)

  FDA approved Lupin Pharmaceuticals' generic clobetasol propionate topical product under an Original Application (ANDA 206075).

• FDA approval · 2015-11-06
  FDA Approved: DESOXIMETASONE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)

  The FDA approved a supplemental application for desoximetasone by Sun Pharmaceutical Industries, enabling changes to the product's labeling …

• FDA approval · 2015-09-02
  FDA Approved: FLUOCINOLONE ACETONIDE — Original Application (Lupin Pharmaceuticals,Inc.)

  FDA approved the original application for a generic fluocinonide acetonide topical product by Lupin Pharmaceuticals (ANDA 206422).

• FDA approval · 2015-06-16
  FDA Approved: DESONIDE — Supplemental Application (Cosette Pharmaceuticals, Inc.)

  The FDA approved a supplemental application for desonide submitted by Cosette Pharmaceuticals, Inc.

• FDA approval · 2015-04-20
  FDA Approved: DESOXIMETASONE — Original Application (Padagis Israel Pharmaceuticals Ltd)

  FDA approved the original application for desoximetasone from Padagis Israel Pharmaceuticals Ltd, granting approval for a topical corticoste…

• FDA approval · 2015-04-15
  FDA Approved: DESOXIMETASONE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)

  FDA approved a supplemental application for desoximetasone submitted by Sun Pharmaceutical Industries, Inc.

• FDA approval · 2015-04-13
  FDA Approved: TRIAMCINOLONE ACETONIDE — Original Application (Padagis Israel Pharmaceuticals Ltd)

  FDA approved Triamcinolone Acetonide via an Original Application (ANDA) for Padagis Israel Pharmaceuticals Ltd., authorizing a generic corti…

• FDA approval · 2015-01-22
  FDA Approved: HYDROCORTISONE — Supplemental Application (Allegis Holdings LLC)

  FDA approved a supplemental application for HYDROCORTISONE lotion from Allegis Holdings LLC.

• 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…