The final monograph (FM) for over-the-counter nasal decongestant drug products will include phenylephrine bitartrate (PEB) individually and in combination drug products in an effervescent dosage form, FDA states in a final rule published in the Federal Register Aug. 1. Additionally, FDA is "expanding" the definition of the term "effervescent tablet" that appeared in the proposed rule with the new term "effervescent dosage form." The agency is making the change "to provide greater formulation flexibility to permit other effervescent dosage forms to be marketed....the pharmacokinetic data provided for the PEB effervescent tablet dosage form would also support use of an effervescent granule or powder dosage form," the notice states. The agency also concludes phenylephrine hydrochloride and PEB can be used interchangeably due to similar safety and efficacy profiles. FDA proposed the monograph amendment in November 2004 (1"The Tan Sheet" Nov. 8, 2004, p. 11). Alka-Seltzer marketer Bayer submitted comments supporting the amendment to the monograph in February 2005 (2"The Tan Sheet" Feb. 14, 2005, p. 7)...
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Pink Sheet for daily insights
Advanz Pharma would have had to show that the European Commission’s decision to revoke Ocaliva’s conditional marketing approval risked causing serious and irreparable harm, according to lawyers from Van Bael & Bellis.
We are conducting a survey to better understand our subscribers’ content and delivery needs. If there are any changes you’d like to see in coverage topics, article format, or the method in which you access the Pink Sheet – or if you love it how it is – now is the time to have your voice heard.
The proportion of China-originated drugs granted expedited reviews in China doubled in the first half of this year, Pharmaprojects data show, surpassing those receiving similar treatment in the US and likely driven by multiple factors.
The FDA recommended removal of a voluntary hold on shipments of the gene therapy to younger patients after finding that the death of an 8-year-old boy in Brazil was unrelated to Elevidys. Discussions on safety of DMD treatment for non-ambulatory patients is ongoing.
While the 15% rate is a substantial blow for pharmaceutical firms, the US-EU deal provides a framework for trade agreements with other countries that could see the industry avoiding higher tariffs elsewhere.