Dermatitis
📧 Sign up to get email alerts when something new happens for Dermatitis.
Sign up freeTop drugs studied for this disease
-
FDA approval · 2014-07-18FDA 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 · 2014-07-14FDA 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 · 2014-06-19FDA Approved: DESOXIMETASONE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
The FDA approved a supplemental application for Desoximetasone from Sun Pharmaceutical Industries, indicating approval of a supplemental for…
-
FDA approval · 2014-05-15FDA 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 · 2014-05-12FDA Approved: DESOXIMETASONE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
The FDA has approved a supplemental application for Desoximetasone from Sun Pharmaceutical Industries, Inc.
- Want full summaries, importance scores, and drug timelines? Upgrade to Plus or Pro.
-
FDA approval · 2014-04-17FDA Approved: ALCLOMETASONE DIPROPIONATE — Supplemental Application (Glenmark Pharmaceuticals Inc., USA)
FDA approved a supplemental application for alclometasone dipropionate by Glenmark Pharmaceuticals, approving changes to the product labelin…
-
FDA label_change · 2014-04-02FDA Approved: HALOG — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
FDA supplemental application for HALOG (halcinonide cream) submitted by Sun Pharmaceutical Industries, Inc., with the submission status indi…
-
FDA approval · 2013-09-20FDA Approved: DESOXIMETASONE — Original Application (Glenmark Pharmaceuticals Inc., USA)
FDA approved Glenmark's desoximetasone for topical use under an Original Application (ANDA), expanding available generic corticosteroid opti…
-
FDA approval · 2013-08-09FDA 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 · 2013-08-09FDA Approved: FLUOCINOLONE ACETONIDE — Original Application (Padagis Israel Pharmaceuticals Ltd)
FDA approved a generic topical fluocinonide acetonide product under an original application from Padagis Israel Pharmaceuticals Ltd.
-
FDA approval · 2013-07-23FDA 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 · 2013-04-11FDA Approved: DESOXIMETASONE — Original Application (Sun Pharmaceutical Industries, Inc.)
FDA approved Sun Pharmaceutical's desoximetasone topical product under an Original Application for the treatment of inflammatory and pruriti…
-
CLINICAL_TRIALS research · 2013-03-22Clinical Trial Update: Evaluation of Irritancy/Allergic Sensitivity to Natural Personal-care Products by Patch Tests [NA]
Clinical trial evaluating irritancy and allergic sensitivity to natural personal-care products via patch tests; current status is unknown.
-
FDA approval · 2013-03-20FDA Approved: DESOXIMETASONE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
FDA approved a supplemental application for desoximetasone from Sun Pharmaceutical Industries, Inc., resulting in an updated approval for th…
-
FDA approval · 2012-11-26FDA Approved: BETAMETHASONE VALERATE — Original Application (Padagis Israel Pharmaceuticals Ltd)
FDA approved a generic topical betamethasone valerate product from Padagis Israel Pharmaceuticals Ltd (Original Application).
-
FDA approval · 2012-08-17FDA 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.
-
FDA approval · 2012-08-09FDA Approved: CLOBETASOL PROPIONATE — Original Application (Padagis Israel Pharmaceuticals Ltd)
FDA approved the original application for clobetasol propionate topical product (a generic) from Padagis Israel Pharmaceuticals Ltd under AN…
-
FDA approval · 2012-06-28FDA Approved: MICORT HC CREAM — Supplemental Application (Legacy Pharma USA Inc.)
FDA approved a supplemental application for MICORT HC CREAM (hydrocortisone acetate cream) from Legacy Pharma USA Inc., representing an appr…
-
FDA approval · 2012-01-05FDA Approved: DESOXIMETASONE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
The FDA approved a supplemental application for Desoximetasone (Sun Pharmaceutical Industries, Inc.). The approval updates the product's lab…
-
FDA approval · 2012-01-03FDA Approved: DESOXIMETASONE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
FDA approved a supplemental application for Desoximetasone from Sun Pharmaceutical Industries, Inc., resulting in changes to the product lab…
-
CLINICAL_TRIALS trial_result · 2011-12-21Clinical Trial Update: Ethanol-Free Clobetasol Propionate Foam 0.05% (Olux-E Foam) vs Vehicle Foam in the Treatment of Chronic Hand Dermatitis. [Phase 4]
This Phase 4 study evaluated ethanol-free clobetasol propionate foam 0.05% versus vehicle foam in adults with chronic hand dermatitis; resul…
-
CLINICAL_TRIALS trial_result · 2011-08-04Clinical Trial Update: Multi-Centre European Photopatch Test Study [NA]
A completed multicenter European photopatch test study investigating photocontact dermatitis.
-
FDA approval · 2011-07-26FDA Approved: ALCLOMETASONE DIPROPIONATE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
FDA approved a supplemental application for aclometasone dipropionate from Sun Pharmaceutical Industries, Inc. The approval confirms the cha…
-
FDA approval · 2010-08-20FDA Approved: PROCTOZONE-HC — Original Application (Rising Pharma Holdings, Inc.)
FDA approved Rising Pharma's PROCTOZONE-HC (hydrocortisone 2.5%), an original ANDA for a generic topical corticosteroid product. The approva…
-
CLINICAL_TRIALS trial_result · 2009-11-13Clinical Trial Update: A Randomised Clinical Trial in a Population of Health Care Workers With Hand Eczema [NA]
This document is an update on a randomized clinical trial involving health care workers with hand eczema; the current status of the trial is…