29 November 2017 - TherapeuticsMD announced today that it has resubmitted the new drug application for TX-004HR, the company’s investigational applicator-free estradiol vaginal softgel capsule for the treatment of moderate-to-severe vaginal pain during sexual intercourse (dyspareunia), a symptom of vulvar and vaginal atrophy due to menopause, with the U.S. FDA.

The Company expects to learn of the acceptance of the resubmission within 30 calendar days. The FDA will classify the resubmission as Class 1 or Class 2 upon acceptance of the resubmission. A Class 1 review constitutes a two-month review from the date of resubmission and a Class 2 review constitutes a six-month review from the date of resubmission.

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