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Industry Dynamics

Industry News

05-17

2021

Heron Therapeutics Announces U.S. FDA Approval of ZYNRELEF? (HTX-011) for the Management of Postoperative Pain for up to 72 Hours

May 23, 2022 -- Heron Therapeutics, Inc. today announced that the U.S. Food and Drug Administration (FDA) has approved ZYNRELEF (bupivacaine and meloxicam) extended-release solution for use in adults for soft tissue or p……

04-23

2021

U.S. Food and Drug Administration Approves Opdivo? (nivolumab) in Combination with Chemotherapy for Patients with Advanced or Metastatic Gastric Cancer, Gastroesophageal Junction Cancer, and Esophageal Adenocarcinoma, Regardless of PD-L1 Expression Status

April 26, 2022—Bristol Myers Squibb today announced that Opdivo (nivolumab) (injection for intravenous use), in combination with fluoropyrimidine- and platinum-containing chemotherapy, was approved by the U.S. Food and D……

04-09

2021

Supernus Announces FDA Approval of Qelbree (SPN-812) for the Treatment of ADHD

April 02, 2022-- Supernus Pharmaceuticals, Inc. (Nasdaq: SUPN), a biopharmaceutical company focused on developing and commercializing products for the treatment of central nervous system (CNS) diseases, today announced t……

03-31

2021

Jazz Pharmaceuticals Announces FDA Approval of Additional Indication for Vyxeos? (daunorubicin and cytarabine) for the Treatment of Secondary Acute Myeloid Leukemia in Pediatric Patients

March 30, 2022—Jazz Pharmaceuticals plc (Nasdaq: JAZZ) today announced that the U.S. Food and Drug Administration (FDA) approved a revised label for Vyxeos? (daunorubicin and cytarabine) to include a new indication to tr……

03-12

2021

AVEO Oncology Announces U.S. FDA Approval of FOTIVDA? (tivozanib) for the Treatment of Adult Patients with Relapsed or Refractory Advanced Renal Cell Carcinoma

Mar. 20, 2022-- AVEO Oncology (Nasdaq: AVEO) today announced that the U.S. Food and Drug Administration (FDA) has approved FOTIVDA? (tivozanib) for the treatment of adults with relapsed or refractory advanced renal cell ……

02-26

2021

Novartis Entresto? granted expanded indication in chronic heart failure by FDA

February 26, 2022 — Novartis today announced that the US Food and Drug Administration (FDA) has approved the following expanded indication for Entresto? (sacubitril/valsartan): to reduce the risk of cardiovascular death ……

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