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filingDate 2017-10-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2019-11-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2019532109-A
titleOfInvention Lyophilized pharmaceutical composition for vaginal delivery
abstract As used herein, an effective amount of at least one active ingredient, a crystal structure-forming agent in an amount of about 5% to about 40% by weight, based on the total weight of the lyophilized dosage form, and at least one mucoadhesive agent Disclosed is a solid lyophilized vaginal dosage form that may have a polymeric matrix forming agent. The pH of the dosage form can be about 4.0-5.0 and can disintegrate within 120 seconds after contacting the vaginal mucosa. A method of delivering the active ingredient to the vaginal mucosa using the disclosed solid dosage forms is also described.
priorityDate 2016-10-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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