InvestorsHub Logo
Post# of 252019
Next 10
Followers 2
Posts 117
Boards Moderated 0
Alias Born 12/07/2011

Re: biomaven0 post# 178865

Friday, 06/06/2014 12:18:47 PM

Friday, June 06, 2014 12:18:47 PM

Post# of 252019
In my view, the only possible reason they could have for obtaining an NDC was to deceive naive investors by enabling their PR.

Total garbage! Any homeopathic product that is sold in the U.S must have an NDC number. It isn't optional:

http://www.fda.gov/downloads/AboutFDA/WorkingatFDA/FellowshipInternshipGraduateFacultyPrograms/PharmacyStudentExperientialProgramCDER/UCM255181.pdf

As is made clear in the article, the term "drug" includes:

(A) articles recognized in the official United States Pharmacopeia, official Homeopathic Pharmacopeia of the United States, or official National Formulary, or any supplement to any of them



The PR just confirms that this necessary step in preparing the product for sale is complete. The company is making a factual statement that by obtaining an NDC, it is in compliance with FDA requirements and that Emesyl can begin the manufacturing phase. Where is the attempt to deceive ? I don't see any words implying that the FDA has "approved" this product ?

Are you suggesting that the company should not have announced that it had obtained an NDC for Emesyl for fear that investors might misconstrue the information and think that the product had FDA approval ? If not, how do you think the company should have communicated the fact that it had obtained an NDC ? Is it unimportant that investors should be made aware of hurdles that are being crossed in the process of preparing Emesyl for public sale?


Join the InvestorsHub Community

Register for free to join our community of investors and share your ideas. You will also get access to streaming quotes, interactive charts, trades, portfolio, live options flow and more tools.