The FDA has accepted a supplemental New Drug Application submitted by Teva (NYSE:TEVA) and Medincell (OTC:MDCLF) for Uzedy ...
Teva Pharmaceuticals (TEVA) and Medincell (MEDCL) announced that the supplemental New Drug Application sNDA for UZEDY extended-release ...
The company is leaning on its subcutaneous technology to deliver long-acting options that could prevent patients from cycling through drugs.
Pharmaceuticals, a U.S. affiliate of Teva Pharmaceutical Industries, and Medincell announced that the supplemental New Drug ...
Parsippany, New Jersey Thursday, February 27, 2025, 13:00 Hrs [IST] ...
Israel-headquartered Teva Pharmaceutical Industries’ US subsidiary and France’s and Medincell announced that the supplemental ...
Other factors he attributed for the lower profit guidance included the immediate hit this year to Teva’s schizophrenia drug, Uzedy, from the Medicare Part D redesign under the Inflation Reduction Act; ...
Teva Pharmaceutical Industries Limited develops ... associated with Huntington’s disease and tardive dyskinesia; UZEDY for the treatment of schizophrenia; ProAir RespiClick inhalation powder ...
(RTTNews) - Teva Pharmaceutical Industries Limited (TEVA) and Medincell (MEDCL) announced that the FDA has accepted their supplemental New Drug Application, or sNDA, for UZEDY extended-release ...
The application leverages existing clinical data for Uzedy along with prior FDA findings on the safety of Udezy in patients ...
UZEDY is currently approved for use every one or two months as a subcutaneous long-acting injectable (LAI) for the treatment ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results