MERCK SERONO ANNOUNCES US FDA APPROVAL FOR FERTILITY PEN (ENG)
(The following press release from Merck KGaA was received by e-mail. It was not confirmed by the sender.)
Your Contact Bettina Frank Phone +49 6151 72-4660
Merck Serono Announces US FDA Approval for Fertility Pen
• Gonal-f® RFF Redi-jectTM (follitropin alfa injection) redesigned to incorporate patient and provider feedback
Darmstadt, Germany, October 18, 2013 - Merck Serono, the biopharmaceutical division of Merck, today announced that the U.S. Food and Drug Administration (FDA) granted approval to its subsidiary, EMD Serono, Inc., for Gonal-f® RFF Redi-ject™ (follitropin alfa injection), a disposable pre-filled drug injector pen intended for the subcutaneous injection of a liquid formulation of Gonal-f® RFF (Revised Formulation Female).
The complete news release can be downloaded at the following link: http://news.merck.de/N/0/5984B5487B5D4240C1257C080052D73C/$File/PR_Gonal_FDA_e.p df
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Merck KGaA ,Darmstadt, Germany External Communications E-mail: Media.Relations@merck.de Hotline: +49 (0) 6151/72-5000
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