Clarinex-D 12 Hour is a brand name of desloratadine/pseudoephedrine, approved by the FDA in the following formulation(s):
CLARINEX-D 12 HOUR (desloratadine; pseudoephedrine sulfate - tablet, extended release; oral)
Manufacturer: SCHERING
Approval date: February 1, 2006
Strength(s): 2.5MG;120MG [RLD]
Has a generic version of Clarinex-D 12 Hour been approved?
No. There is currently no therapeutically equivalent version of Clarinex-D 12 Hour available.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Clarinex-D 12 Hour. 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.
8-chloro-6,11-dihydro-11- ] (4-piperidylidine)-5H-benzo[5,6]cyclohepta[1,2-bpyridine oral compositions
Patent 6,100,274
Issued: August 8, 2000
Inventor(s): Kou; Jim H.
Assignee(s): Schering Corporation
Stable pharmaceutical compositions containing 8-chloro-6,11-dihydro-11-(4-piperidylidene)-5H-benzo[5,6]cycloheptic[1,2-b ]pyridine("DCL") and a DCL protective amount of a pharmaceutically acceptable basic salt such as calcium dibasic phosphate and an amount of at least one disintegrant, preferably two disintegrates such as microcrystalline cellulose and starch sufficient to provide dissolution of at least about 80% by weight of the pharmaceutical composition in about 45 minutes and suitable for oral administration to treat allergic reactions in mammals such as man are disclosed.Patent expiration dates:
- July 7, 2019✓
- January 7, 2020✓
- July 7, 2019
Extended release oral dosage composition
Patent 6,709,676
Issued: March 23, 2004
Inventor(s): Wing-Kee Philip; Cho
Assignee(s): Schering Corporation
A bilayer solid composition comprising (a) an immediate release first layer comprising an anti-allergic effective amount of desloratadine and at least one pharmaceutically acceptable excipient and (b) a sustained release second layer comprising an effective amount of a nasal decongestant, e.g. pseudoephedrine sulfate and a pharmaceutically acceptable sustained release agent wherein the composition contains less than about 2% of desloratadine decomposition products is disclosed. A solid composition comprising an anti-allergic effective amount of desloratadine and at least one, and preferably two pharmaceutically acceptable antioxidants is also disclosed.Patent expiration dates:
- February 18, 2021✓✓
- February 18, 2021
Compositions of descarboethoxyloratadine
Patent 7,214,683
Issued: May 8, 2007
Inventor(s): Aberg; A. K. Gunnar & McCullough; John R. & Smith; Emil R.
Assignee(s): Sepracor Inc.
Methods are disclosed utilizing DCL, a metabolic derivative of loratadine, for the treatment of allergic rhinitis, and other disorders, while avoiding the concomitant liability of adverse side-effects associated with other non-sedating antihistamines.Patent expiration dates:
- December 30, 2014✓
- June 30, 2015✓
- December 30, 2014
Methods for the treatment of allergic rhinitis
Patent 7,214,684
Issued: May 8, 2007
Inventor(s): Aberg; A. K. Gunnar & McCullough; John R. & Smith; Emil R.
Assignee(s): Sepracor Inc.
Methods are disclosed utilizing DCL, a metabolic derivative of loratadine, for the treatment of allergic rhinitis, and other disorders, while avoiding the concomitant liability of adverse side-effects associated with other non-sedating antihistamines.Patent expiration dates:
- December 30, 2014✓
- June 30, 2015✓
- December 30, 2014
Extended release oral dosage composition
Patent 7,618,649
Issued: November 17, 2009
Inventor(s): Cho; Wing-Kee Philip
Assignee(s): Schering Corporation
A bilayer solid composition comprising (a) an immediate release first layer comprising an anti-allergic effective amount of desloratadine and at least one pharmaceutically acceptable excipient and (b) a sustained release second layer comprising an effective amount of a nasal decongestant, e.g. pseudoephedrine sulfate and a pharmaceutically acceptable sustained release agent wherein the composition contains less than about 2% of desloratadine decomposition products is disclosed. A solid composition comprising an anti-allergic effective amount of desloratadine and at least one, and preferably two pharmaceutically acceptable antioxidants is also disclosed.Patent expiration dates:
- December 19, 2020✓✓
- June 19, 2021✓
- December 19, 2020
See also...
- Clarinex-D 12 Hour Consumer Information (Drugs.com)
- Clarinex-D 12 Hour Sustained-Release Tablets Consumer Information (Wolters Kluwer)
- Clarinex-D 12 Hour Consumer Information (Cerner Multum)
- Desloratadine/Pseudoephedrine Sustained-Release Tablets Consumer Information (Wolters Kluwer)
- Desloratadine and pseudoephedrine Consumer Information (Cerner Multum)
- Clarinex-D Advanced Consumer Information (Micromedex)
- Desloratadine and pseudoephedrine Advanced Consumer Information (Micromedex)
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