Xanodyne Pharmaceuticals

Xanodyne Pharmaceuticals

Pharmaceuticals, 1 Riverfront Pl Ste 900, Newport, Kentucky, 41071, United States, 51-200 Employees

xanodyne.com

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phone no 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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  • 1 Riverfront Pl Ste 900, Newport, Kentucky, 41071, United States Headquarters: 1 Riverfront Pl Ste 900, Newport, Kentucky, 41071, United States
  • 51-200 Employees: 51-200
  • dollar-icon Revenue: $50 Million to $100 Million

industries-icon Industry: Pharmaceuticals

SIC 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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