pharmaphorum

JUNE 3, 2021

The FDA approval of Alkermes’ new antipsychotic drug Lybalvi couldn’t have gone any better for the company, but it could still face a big challenge positioning the new drug in the highly genericised market. The post After FDA approval, Alkermes plans soft launch for antipsychotic Lybalvi appeared first on.

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The Checkup by Singlecare

SEPTEMBER 7, 2023

Lexapro was approved by the United States Food and Drug Administration (FDA) in 2002. A Lexapro generic, called escitalopram, has been available since 2012. Continue reading to learn more about Lexapro and its generic escitalopram. What are the differences between brand name and generic Lexapro? In 2020, an estimated 6.3

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The Checkup by Singlecare

OCTOBER 12, 2023

Abilify generic | Abilify vs. aripiprazole | Cost | Off-label use | How to switch Abilify is a brand-name medication approved to treat certain mental health conditions, including the treatment for schizophrenia , bipolar disorder , and major depressive disorder. Abilify first received FDA approval in 2002. mL, 960 mg/3.2

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The Checkup by Singlecare

JULY 17, 2023

Food Drug Administration (FDA) , a generic medicine works in the same way and provides the same clinical benefit as brand-name medicine. Generic medications must have the same dosage form, safety, strength, route of administration, quality, performance characteristics, and intended use. How much is generic Zoloft?

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The Checkup by Singlecare

AUGUST 5, 2023

Yes, there is a generic version of Cialis available called tadalafil. Generic Cialis became available in the United States after the exclusivity patent for Cialis , held by Eli Lilly, expired in 2018. As a generic medicine, tadalafil offers the same benefits and uses as Cialis but typically at a lower price.

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pharmaphorum

JANUARY 30, 2023

Moreover, more than any other medicine, antibiotics are more likely to face insufficient supply, with analysis by the US Pharmacopeia suggesting they are 42% more likely to be in shortage compared to all other drugs. Larger questions remain around the way in which to support manufacturers to invest in production capabilities for antibiotics.

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pharmaphorum

MAY 26, 2022

Despite policies, guidelines, and regulations to promote the diversification of clinical trial groups by the European Medicines Agency (EMA) and FDA, the inclusion of key demographic populations within clinical research continues to be less than proportionate to their representation in society.

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