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February 1, 2023

IBSA Pharma Inc. Issues Voluntary Nationwide Recall of Select Lots of TIROSINT® -SOL (levothyroxine sodium) Oral Solution Due to Subpotency

February 01, 2023 - IBSA Pharma Inc. is voluntarily recalling 27 lots of TIROSINT®-SOL (levothyroxine sodium) Oral Solution to the consumer level
February 1, 2023

Shop Me Ca Recalls “Diep Bao Cream” Because of Possible Health Risk

February 01, 2023 - Shop Me Ca of Herndon, VA is recalling its 10-gram tubes of “Diep Bao Cream” because they have the potential to be contaminated with lead
February 1, 2023

FDA Approves Jesduvroq (daprodustat) for Anemia Caused by Chronic Kidney Disease for Adults on Dialysis

February 1, 2023 - The U.S. Food and Drug Administration approved Jesduvroq tablets (daprodustat) as the first oral treatment for anemia (decreased number of red
January 31, 2023

New guidance for industry: M13A Bioequivalence for Immediate-Release Solid Oral Dosage Forms

January 31, 2023 - FDA published draft guidance for industry, “M13A Bioequivalence for Immediate- Release Solid Oral Dosage Forms
January 30, 2023

FDA has approved Orserdu for the treatment of postmenopausal

January 30th, 2023 – The Menarini Group, a leading Italian pharmaceutical and diagnostics company, has announced that the U.S. Food and Drug Administration
January 27, 2023

Jaypirca (pirtobrutinib) approved for Adult Patients with Relapsed or Refractory Mantle Cell Lymphoma

January 27, 2023 - Loxo@Lilly, the oncology unit of Eli Lilly and Company announced that the U.S. Food and Drug Administration approved Jaypirca
January 23, 2023

Brukinsa (zanubrutinib) Approved in the U.S. for Chronic Lymphocytic Leukemia

January 23, 2023 - The U.S. Food and Drug Administration has approved zanubrutinib (Brukinsa), manufactured by the biotechnology company BeiGene, which is a next-generation BTK inhibitor
January 23, 2023

FDA Approves Brenzavvy (bexagliflozin) for the Treatment of Adults with Type 2 Diabetes

January 23, 2023 - TheracosBio has announced that the U.S. Food and Drug Administration (FDA) has approved Brenzavvy (bexagliflozin), an oral sodium-glucose
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Global Reach Health administrates five separate divisions to deliver seamless cross border healthcare solutions and services for a myriad of clients around the globe including insurers, pharmacies, hospitals and clinics, assistance firms, cost containment companies, third party administrators plus public entities and private corporations.

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