See also: Generic Seroquel
Seroquel XR is a brand name of quetiapine, approved by the FDA in the following formulation(s):
SEROQUEL XR (quetiapine fumarate - tablet, extended release; oral)
Manufacturer: ASTRAZENECA
Approval date: May 17, 2007
Strength(s): EQ 200MG BASE [RLD], EQ 300MG BASE, EQ 400MG BASE, EQ 50MG BASE
Manufacturer: ASTRAZENECA
Approval date: August 11, 2008
Strength(s): EQ 150MG BASE
Has a generic version of Seroquel XR been approved?
No. There is currently no therapeutically equivalent version of Seroquel XR available.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Seroquel XR. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.
See also: About generic drugs.
Related Patents
Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.
Novel dibenzothiazepine antipsychotic
Patent 4,879,288
Issued: November 7, 1989
Inventor(s): Warawa; Edward J. & Migler; Bernard M.
Assignee(s): ICI Americas Inc.
11-[4-[2-(2-Hydroxyethoxy)ethyl]-1-piperazinyl]dibenzo[b,f][1,4 ]thiazepine is disclosed as a neuroleptic with a much reduced incidence of side effects such as acute dystonia and dyskinesia and tardive diskinesia.Patent expiration dates:
- September 26, 2011✓✓✓
- September 26, 2011✓✓✓
- September 26, 2011✓✓✓
- March 26, 2012✓
- September 26, 2011
Pharmaceutical compositions using thiazepine
Patent 5,948,437
Issued: September 7, 1999
Inventor(s): Parikh; Bhavnish Vinod & Timko; Robert Joseph & Addicks; William Joseph
Assignee(s): Zeneca Limited
The invention relates to sustained release formulations comprising 11-›4-›2-(2-hydroxyethoxy)ethyl!-1-piperazinyl!dibenzo›b,f! ›1,4!thiazepine or a pharmaceutically acceptable salt thereof, to methods of treating psychotic states and hyperactivity utilizing the sustained release formulations and to a process for preparing the sustained release formulations.Patent expiration dates:
- May 28, 2017✓✓
- May 28, 2017✓✓
- May 28, 2017✓✓
- November 28, 2017✓
- May 28, 2017
Related Exclusivities
Exclusivity is exclusive marketing rights granted by the FDA upon approval of a drug and can run concurrently with a patent or not. Exclusivity is a statutory provision and is granted to an NDA applicant if statutory requirements are met.
- Exclusivity expiration dates:
- November 17, 2010 - PEDIATRIC EXCLUSIVITY
- October 8, 2011 - MONOTHERAPY IN THE TREATMENT OF BIPOLAR MANIA
- October 8, 2011 - MONOTHERAPY IN THE TREATMENT OF BIPOLAR DEPRESSION
- October 8, 2011 - ADJUNCTIVE THERAPY IN THE TREATMENT OF BIPOLAR MANIA
- October 8, 2011 - 50 MG TABLET FOR INITIATION OF DOSE TITRATION FOR BIPOLAR DISORDER
- April 8, 2012 - PEDIATRIC EXCLUSIVITY
- December 2, 2012 - ADJUNCTIVE THERAPY IN THE TREATMENT OF MAJOR DEPRESSIVE DISORDER (MDD)
See also...
- Seroquel XR Sustained-Release Tablets Consumer Information (Wolters Kluwer)
- Seroquel XR Consumer Information (Cerner Multum)
- Seroquel XR Advanced Consumer Information (Micromedex)
- Quetiapine Consumer Information (Wolters Kluwer)
- Quetiapine Sustained-Release Tablets Consumer Information (Wolters Kluwer)
- Quetiapine Consumer Information (Cerner Multum)
- Quetiapine Advanced Consumer Information (Micromedex)
- Quetiapine Fumarate AHFS DI Monographs (ASHP)
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