Pink Sheet is part of the Business Intelligence Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC’s registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 8860726.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By


Hatch quizzes FDA on andro

This article was originally published in The Tan Sheet

Executive Summary

"It appears that FDA is not taking action against [androstenedione] products because you can't decide whether it's a supplement or a drug," Sen. Orrin Hatch (R-Utah) tells FDA General Counsel Daniel Troy during an Aug. 1 Senate Judiciary committee hearing on the "Greater Access to Affordable Pharmaceuticals Act." "I'm counting on FDA moving forward on this, to protect the public health," Hatch continued, "because I think this inaction has been going on far too long." Troy promised to relay concerns to FDA Commissioner Mark McClellan, MD/PhD...

Related Content

Andro Classified As Controlled Substance In Senate Bill; DHEA Excluded





Ask The Analyst

Please Note: You can also Click below Link for Ask the Analyst
Ask The Analyst

Your question has been successfully sent to the email address below and we will get back as soon as possible. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts