First Generic Version of NuvaRing Gets FDA Approval

The vaginal ring releases on average 0.12mg/day of etonogestrel, a progestin, and 0.015mg/day of ethinyl estradiol, an estrogen.

The Food and Drug Administration (FDA) has approved EluRyng (etonogestrel/ethinyl estradiol vaginal ring; Amneal), the first generic version of NuvaRing (Merck), for use by females of reproductive age to prevent pregnancy.

The vaginal ring releases on average 0.12mg/day of etonogestrel, a progestin, and 0.015mg/day of ethinyl estradiol, an estrogen. One ring is inserted in the vagina and must remain in place continuously for 3 weeks. It is removed for a 1-week break, during which a withdrawal bleed usually occurs. A new ring is inserted 1 week after the last ring was removed. 

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Each EluRyng is individually packaged in its own pouch; each carton contains 3 pouches. In a press release, Amneal stated that the launch of EluRyng will begin on December 12, 2019.

For more information visit amneal.com.