Arthritis
📧 Sign up to get email alerts when something new happens for Arthritis.
Sign up freeTop drugs studied for this disease
-
EMA approval · 2026-08-19EMA Authorised: Xeljanz (tofacitinib) — Pfizer Europe MA EEIG
Authorisation granted in the EU for Xeljanz (tofacitinib) for arthritis and rheumatoid conditions.
-
EMA approval · 2026-08-18EMA Authorised: Amgevita (adalimumab) — Amgen Europe B.V.
Amgevita (adalimumab) by Amgen Europe B.V. has been authorised by the EMA for multiple inflammatory diseases including arthritis, psoriatic …
-
EMA approval · 2026-07-01EMA Authorised: Erelzi (etanercept) — Sandoz GmbH
Authorised status for Erelzi (etanercept) by Sandoz GmbH, expanding access to therapy for multiple inflammatory arthritis conditions.
-
EMA approval · 2026-06-12EMA Authorised: Apremilast Accord — Accord Healthcare S.L.U.
Accord Healthcare S.L.U. has been authorised in the EU for apremilast (Accord).
-
FDA approval · 2024-08-07FDA Approved: VOLTAREN ARTHRITIS PAIN — Supplemental Application (Haleon US Holdings LLC)
The FDA approved Haleon's supplemental application for Voltaren Arthritis Pain (diclofenac sodium), updating the product labeling to support…
- Want full summaries, importance scores, and drug timelines? Upgrade to Plus or Pro.
-
FDA approval · 2023-02-21FDA Approved: VOLTAREN ARTHRITIS PAIN — Supplemental Application (Haleon US Holdings LLC)
The FDA approved a supplemental application for Voltaren Arthritis Pain (diclofenac sodium) submitted by Haleon US Holdings LLC. This action…
-
FDA approval · 2022-05-31FDA Approved: IBUPROFEN PM — Original Application (KROGER COMPANY)
FDA approved Kroger's Ibuprofen PM, an over-the-counter combination product containing ibuprofen and diphenhydramine citrate, under an origi…
-
FDA approval · 2021-08-25FDA Approved: ARTHRITIS PAIN RELIEVER — Original Application (WALGREENS)
FDA approved Walgreens' Arthritis Pain Reliever as an original ANDA for acetaminophen to relieve arthritis pain.
-
FDA approval · 2020-12-12FDA Approved: VOLTAREN ARTHRITIS PAIN — Supplemental Application (Haleon US Holdings LLC)
The FDA approved a supplemental application for Voltaren Arthritis Pain (diclofenac sodium) to expand labeling for arthritis pain management…
-
FDA approval · 2020-10-23FDA Approved: ARTHRITIS PAIN RELIEVER — Supplemental Application (Publix Super Markets Inc)
FDA approved a supplemental application for Arthritis Pain Reliever containing diclofenac sodium, manufactured by Publix Super Markets Inc.
-
FDA approval · 2020-08-13FDA Approved: ARTHRITIS PAIN RELIEVER — Supplemental Application (CVS PHARMACY, INC)
FDA approved a supplemental application for CVS Pharmacy, Inc.'s Arthritis Pain Reliever diclofenac sodium product.
-
FDA approval · 2020-02-14FDA Approved: VOLTAREN ARTHRITIS PAIN — Supplemental Application (Haleon US Holdings LLC)
FDA approves a supplemental application for Voltaren Arthritis Pain (diclofenac sodium) by Haleon US Holdings LLC to expand the labeling for…
-
FDA approval · 2019-08-16FDA Approved: TOPCARE 8 HR ARTHRITIS PAIN RELIEF — Supplemental Application (Topco Associates LLC)
FDA approved a supplemental application for TOPCARE 8 HR Arthritis Pain Relief (acetaminophen) from Topco Associates LLC.
-
FDA approval · 2019-05-16FDA Approved: ARTHRITIS PAIN RELIEVER — Original Application (Publix Super Markets Inc)
FDA approves the original application for a generic diclofenac sodium product marketed as Arthritis Pain Reliever by Publix Super Markets In…
-
FDA approval · 2019-04-16FDA Approved: 8 HOUR ARTHRITIS PAIN — Original Application (AMERISOURCE BERGEN)
FDA approved the original application for a generic acetaminophen product marketed as 8 HOUR ARTHRITIS PAIN for arthritis pain by Amerisourc…
-
FDA approval · 2019-01-16FDA Approved: TYLENOL 8 HR ARTHRITIS PAIN — Supplemental Application (Kenvue Brands LLC)
FDA approves a supplemental application for Tylenol 8 Hour Arthritis Pain (acetaminophen) by Kenvue Brands LLC, updating its labeling for ar…
-
FDA approval · 2018-05-31FDA Approved: ARTHRITISPAIN RELIEF — Original Application (P & L Development, LLC)
FDA approved an original application for ARTHRITISPAIN RELIEF containing acetaminophen, manufactured by P & L Development, LLC.
-
FDA approval · 2016-08-26FDA Approved: TYLENOL 8 HR ARTHRITIS PAIN — Supplemental Application (Kenvue Brands LLC)
Supplemental application approved for TYLENOL 8 HR ARTHRITIS PAIN (acetaminophen) by Kenvue Brands LLC.
-
FDA approval · 2016-01-10FDA Approved: TOPCARE 8 HR ARTHRITIS PAIN RELIEF — Supplemental Application (Topco Associates LLC)
FDA approved a supplemental application for TOPCARE 8 HR Arthritis Pain Relief (acetaminophen) from Topco Associates LLC, authorizing the pr…
-
FDA approval · 2015-10-28FDA Approved: ALEVE PM — Supplemental Application (Bayer HealthCare LLC.)
FDA approved a supplemental application for ALEVE PM (diphenhydramine hydrochloride and naproxen sodium) to support its continued marketing …
-
FDA approval · 2015-05-11FDA Approved: VOLTAREN ARTHRITIS PAIN — Supplemental Application (Haleon US Holdings LLC)
The FDA approved a supplemental application for Voltaren Arthritis Pain (diclofenac sodium) submitted by Haleon US Holdings LLC.
-
FDA approval · 2014-12-23FDA Approved: TYLENOL 8 HR ARTHRITIS PAIN — Supplemental Application (Kenvue Brands LLC)
FDA approved a supplemental application for Tylenol 8 Hour Arthritis Pain (acetaminophen) from Kenvue Brands LLC.
-
FDA approval · 2014-12-12FDA Approved: TYLENOL 8 HR ARTHRITIS PAIN — Supplemental Application (Kenvue Brands LLC)
FDA approved a supplemental application for Tylenol 8 Hour Arthritis Pain (acetaminophen) from Kenvue Brands LLC.
-
FDA approval · 2014-09-29FDA Approved: VOLTAREN ARTHRITIS PAIN — Supplemental Application (Haleon US Holdings LLC)
The FDA approved a supplemental application to Voltaren Arthritis Pain (diclofenac sodium) to expand its labeling with a new indication for …
-
FDA approval · 2014-03-06FDA Approved: TYLENOL 8 HR ARTHRITIS PAIN — Supplemental Application (Kenvue Brands LLC)
The FDA approved a supplemental application for Tylenol 8 Hour Arthritis Pain (acetaminophen) from Kenvue Brands LLC.