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The drug is typically indicated to have superior efficacy over other existing antipsychotics for the treatment of bipolar disorder, followed by olanzapine and aripiprazole, in that order. Quetiapine is currently the only antipsychotic to produce equal efficacy as a standalone therapy for mixed manic-depressive mood swings as it is when used in ...
Maybe some research about the exclusivity status of Seroquel XR should be done. The "Dosage" section mentions 2017 as the year of expiration of such exclusivity. However, I just got my refill for 150mg tablets, and got a Generic made by Teva, and named Teva Quetiapine XR. Update: Here are some links about the subject.
Teva Pharmaceutical Industries Ltd. (also known as Teva Pharmaceuticals) is an Israeli multinational pharmaceutical company. Teva specializes primarily in generic drugs, but other business interests include branded-drugs, active pharmaceutical ingredients (APIs) and, to a lesser extent, contract manufacturing services and an out-licensing ...
AstraZeneca agreed to pay $3.1 million to settle a New York State Attorney General's lawsuit saying the British pharmaceutical company improperly promoted and marketed the schizophrenia drug ...
With a legacy of more than 100 years, the Better Business Bureau (BBB) is the go-to watchdog for evaluating businesses and charities. The nonprofit organization maintains a massive database of ...
Teva is in the process of recovering from loss of exclusivity to its multiple sclerosis drug Copaxone and a spate of lawsuits, and is betting that a trio of its branded drugs - Austedo, migraine ...
Seroquel: dibenzothiazepine: N05AH04 Remoxipride: Roxiam: salicylamide: N05AL04 Reserpine: ... Generic Name Brand Names Chemical class ATC code Antipsychotic esters
The following are settlements reached with US authorities against pharmaceutical companies to resolve allegations of "off-label" promotion of drugs. Under the Federal Food, Drug, and Cosmetic Act, it is illegal for pharmaceutical companies to promote their products for uses not approved by the Food and Drug Administration (FDA), and corporations that market drugs for off-label indications may ...