Spinal Cord Injury
📧 Sign up to get email alerts when something new happens for Spinal Cord Injury.
Sign up freeTop drugs studied for this disease
-
FDA approval · 2014-12-14FDA Approved: TIZANIDINE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
The FDA approved a supplemental application for a generic tizanidine product from Sun Pharmaceutical Industries under an ANDA. Tizanidine is…
-
FDA approval · 2014-08-29FDA Approved: ZANAFLEX — Supplemental Application (Covis Pharma US, Inc)
The FDA approved a supplemental application for ZANAFLEX (tizanidine hydrochloride) submitted by Covis Pharma US, Inc.
-
FDA approval · 2013-11-07FDA Approved: ZANAFLEX — Supplemental Application (Covis Pharma US, Inc)
FDA approved a supplemental application for ZANAFLEX (tizanidine hydrochloride) from Covis Pharma US, Inc., indicating a labeling update as …
-
FDA approval · 2013-03-19FDA Approved: ZANAFLEX — Supplemental Application (Covis Pharma US, Inc)
FDA approved a supplemental application for ZANAFLEX (tizanidine hydrochloride) from Covis Pharma US, Inc.
-
FDA approval · 2013-03-08FDA Approved: ZANAFLEX — Supplemental Application (Covis Pharma US, Inc)
The FDA approved a supplemental application for Zanaflex (tizanidine hydrochloride) submitted by Covis Pharma US, Inc., updating the labelin…
- Want full summaries, importance scores, and drug timelines? Upgrade to Plus or Pro.
-
FDA approval · 2013-03-06FDA Approved: LIORESAL (BACLOFEN) — Supplemental Application (Amneal Pharmaceuticals LLC)
FDA approved a supplemental application for Lioresal (baclofen) from Amneal Pharmaceuticals LLC, enabling changes to the product labeling fo…
-
FDA approval · 2012-11-28FDA Approved: TIZANIDINE — Original Application (Unichem Pharmaceuticals (USA), Inc.)
FDA approved Unichem Pharmaceuticals (USA), Inc.'s original abbreviated new drug application for tizanidine, a generic muscle relaxant. This…
-
FDA approval · 2012-02-03FDA Approved: TIZANIDINE HYDROCHLORIDE — Original Application (Apotex Corp.)
FDA approved Apotex Corp.'s generic tizanidine hydrochloride (Original Application) for the treatment of spasticity associated with neurolog…
-
FDA approval · 2011-11-13FDA Approved: LIORESAL (BACLOFEN) — Supplemental Application (Amneal Pharmaceuticals LLC)
FDA approved a supplemental application for Lioresal (baclofen) submitted by Amneal Pharmaceuticals LLC.
-
FDA approval · 2011-06-17FDA Approved: BACLOFEN — Supplemental Application (Upsher-Smith Laboratories, LLC)
The FDA approved Upsher-Smith Laboratories' supplemental application for baclofen, enabling continued availability of this generic product f…
-
FDA approval · 2010-11-19FDA Approved: GABLOFEN — Original Application (Piramal Critical Care Inc)
The FDA approved GABLOFEN (baclofen injection) under an original application from Piramal Critical Care Inc, adding a new injectable baclofe…
-
FDA approval · 2010-04-27FDA Approved: BACLOFEN — Supplemental Application (Northstar RxLLC)
The FDA approved a supplemental application for baclofen submitted by Northstar RxLLC. Baclofen is used to reduce muscle spasticity in condi…
-
FDA approval · 2009-09-18FDA Approved: BACLOFEN — Original Application (Northstar RxLLC)
FDA approved the original ANDA for generic baclofen from Northstar RxLLC. This approval authorizes the generic product for treating spastici…
-
FDA approval · 2009-04-03FDA Approved: BACLOFEN — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
The FDA approved Teva's supplemental application for Baclofen (BACLOFEN), updating the existing approval for the drug.
-
FDA approval · 2009-04-03FDA Approved: BACLOFEN — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
The FDA approved Teva's supplemental application for baclofen (generic), indicating an approval related to the product's labeling or formula…
-
FDA approval · 2008-08-13FDA Approved: BACLOFEN — Supplemental Application (Chartwell RX, LLC)
FDA approved a supplemental application for baclofen submitted by Chartwell RX, LLC under ANDA 077241.
-
FDA approval · 2008-04-02FDA Approved: TIZANIDINE — Supplemental Application (Apotex Corp.)
The FDA approved a supplemental application from Apotex Corp. to market a generic version of tizanidine.
-
FDA approval · 2007-03-22FDA Approved: TIZANIDINE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
FDA approved a supplemental application for tizanidine from Sun Pharmaceutical Industries, Inc.
-
FDA approval · 2007-02-07FDA Approved: TIZANIDINE — Supplemental Application (Dr. Reddy's Laboratories Limited)
FDA approved a supplemental application for tizanidine submitted by Dr. Reddy's Laboratories Limited. The approval indicates regulatory clea…
-
FDA approval · 2006-07-28FDA Approved: ZANAFLEX — Supplemental Application (Covis Pharma US, Inc)
The FDA approved a supplemental NDA for ZANAFLEX (tizanidine hydrochloride) submitted by Covis Pharma US, Inc., resulting in updated labelin…
-
FDA approval · 2006-07-28FDA Approved: ZANAFLEX — Supplemental Application (Covis Pharma US, Inc)
The FDA approved a supplemental application for ZANAFLEX (tizanidine hydrochloride) submitted by Covis Pharma US, Inc.