Xanodyne Pharmaceuticals
Pharmaceuticals, 1 Riverfront Pl Ste 900, Newport, Kentucky, 41071, United States, 51-200 Employees
Phone Number: +19*********
Who is XANODYNE PHARMACEUTICALS
Xanodyne Pharmaceuticals, Inc., founded in 2001, is an integrated specialty pharmaceutical company with both development and commercial capabilities focused on women's healthcare and pain...
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- Headquarters: 1 Riverfront Pl Ste 900, Newport, Kentucky, 41071, United States
- Employees: 51-200
- Revenue: $50 Million to $100 Million
Industry: Pharmaceuticals
SIC Code: 5122 | NAICS Code: 325412 | Show More
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Frequently Asked Questions Regarding Xanodyne Pharmaceuticals
Answer: Xanodyne Pharmaceuticals's headquarters are located at 1 Riverfront Pl Ste 900, Newport, Kentucky, 41071, United States
Answer: Xanodyne Pharmaceuticals's phone number is +19*********
Answer: Xanodyne Pharmaceuticals's official website is https://xanodyne.com
Answer: Xanodyne Pharmaceuticals's revenue is $50 Million to $100 Million
Answer: Xanodyne Pharmaceuticals's SIC: 5122
Answer: Xanodyne Pharmaceuticals's NAICS: 325412
Answer: Xanodyne Pharmaceuticals has 51-200 employees
Answer: Xanodyne Pharmaceuticals is in Pharmaceuticals
Answer: Xanodyne Pharmaceuticals contact info: Phone number: +19********* Website: https://xanodyne.com
Answer: Xanodyne Pharmaceuticals, Inc., founded in 2001, is an integrated specialty pharmaceutical company with both development and commercial capabilities focused on women's healthcare and pain management. We market a portfolio of revenue generating products consisting of prescription pharmaceuticals and a line of prenatal vitamins, and we are advancing a late stage pipeline of product candidates targeted at significant potential markets in Xanodyne's focus areas. We are developing: ZipsorTM for the treatment of mild to moderate acute pain for which we have received an Approvable Letter from the U.S. Food & Drug Administration (FDA); XP12B for the treatment of menorrhagia (heavy menstrual bleeding) has recently received top line Phase 3 clinical data and NDA filing is being completed; and XP20B for the treatment of mild to moderate pain for which a Phase 3 trial has been completed in the U.S.
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