the present invention provides a composition comprising (i) fexofenadine or a pharmaceutically acceptable salt thereof and (ii) a pharmaceutical excipient that increases the solubility of the fexofenadine or salt in water.
Patents listed in the fda orange book drug database of fexofenadine hydrochloride with information and expiryexpiration dates.
Us8933097b2 us12138,468 us13846808a us8933097b2 us 8933097 b2 us8933097 b2 us 8933097b2 us 13846808 a us13846808 a us 13846808a us 8933097 b2 us8933097 b2 us 8933097b2 authority us united states prior art keywords aqueous pharmaceutical ml volume weight suspension according prior art date legal status (the legal status is an assumption and is.).
The present invention relates to a composition for use as a capsule fill comprising (a) fexofenadine hydrohalide (b) alkali hydroxide, wherein the molar ratio of the alkali hydroxide to fexofenadine is greater than 1. This composition is a stable solution, and comprises a sufficiently high concentration of fexofenadine to be useful for.
Of bioequivalence has determined your fexofenadine hydrochloride.
Fexofenadine is the active metabolite of terfenadine developed by marion merrel dow.
Castañer, fexofenadine hydrochloride, drugs of the future, vol. Preparation of terfenadine and derivatives, wo patent 9833789, 1998.
Fexofenadine hydrochloride inn patent status, expiration and generic drug launch.
7, based on international application wo 9626726, was granted on the.
Fexofenadine hydrochloride c32h40clno2 - structure, chemical names, physical and chemical properties, classification, patents, literature,.
fexofenadine is the active metabolite of terfenadine developed by marion merrel dow.
Also known as allegra, allegra allergy, mucinex allergy, aller-ease, allegra odt, allegra hives the following information is not intended to endorse drugs or recommend therapy. While these reviews might be helpful, they are not a substitute for the expertise, skill, knowledge and judgement of healthcare practitioners in patient care.
The present invention provides an immediate release oral pharmaceutical composition comprising a therapeutically effective amount of fexofenadine or its. Fexofenadine undergoes negligible metabolism (hepatic or non-hepatic), as it was the only major compound identified in urine and faeces of animals and man. The plasma concentration profiles of fexofenadine follow a bi-exponential decline with a terminal elimination half-life ranging from 11 to 15 hours after multiple dosing.
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