BAUSCH HEALTH COMPANIES WKN: A2JQ1X ISIN: CA0717341071 Forum: Aktien Thema: Hauptdiskussion

https://www.stck.pro/video/BHC/72168293

Biophytis ist aktuell auch sehr interessant, die Zulassung des COVA Programms (Medikamentenzulassung) soll Dezember für Brasilien und Januar für USA kommen. Die Aktie ist aktuell bei 1 Cent zu haben. Auf jedenfall einen Zock Wert 👌🙃 persönliche Meinung.

https://seekingalpha.com/news/3996541-bausch-health-companies-gaap-eps-of-0_07-beats-0_12-revenue-of-2_17b-beats-130m?source=WhatsApp

https://www.marketbeat.com/stocks/NYSE/BHC/earnings/

Ich rechne heute mit 20% plus

https://stocktwits.com/symbol/BHC

🚀

https://seekingalpha.com/news/3972676-bausch-health-soars-after-court-ruling-in-patent-dispute-with-norwich-pharma?

War echt überfällig

https://www.reuters.com/business/bausch-lomb-name-brent-saunders-ceo-wsj-2023-02-15/

Bausch Health (NYSE:BHC) is up 11% after the US FDA issued updated guidance for the company's irritable bowel syndrome with diarrhea drug Xifaxan (rifaximin) that will require generic drugmakers to conduct pharmacokinetic and in vitro bioequivalence studies. According to the guidance, generic drugmakers have two options. They can either conduct four pharmacokinetic bioequivalence studies and in vitro bioequivalence studies (comparative dissolution); or four pharmacokinetic bioequivalence studies, in vitro bioequivalence studies (comparative dissolution), and two clinical endpoint bioequivalence studies. The agency also noted that waiver requests for in vitro testing is "not applicable." The guidance is seen as a blow to companies with rifaximin abbreviated New Drug Applications (ANDAs) seeking to get their products onto the market. In September, the FDA granted tentative approval to Norwich Pharmaceuticals' rifaximin ANDA. In July, a federal judge issued an order in favor of Norwich in a patent dispute on Xifaxan with Bausch Health (BHC).

FDA Update

Gerüchteküche...es geht steil hoch

Wow steigt gut heute

Bausch expects Xifaxan patent to hinder generic entry in US until 2029 despite approval https://seekingalpha.com/news/3881587-bausch-expects-xifaxan-generic-to-not-enter-market-until-2029-despite-approval-due-to-patent-protection?source=WhatsApp

https://www.thestreet.com/quote/BHC