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  • POWDER;INTRAVENOUS - EQ 250MG BASE/VIAL;250MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • POWDER;INTRAVENOUS - EQ 500MG BASE/VIAL;500MG/VIAL

https://endpts.com/merck-defends-antibiotics-approval-from-2019-as-bmj-investigation-points-to-decline-in-fda-standards/

Zachary Brennan ENDPTS
17 May 2023

https://www.pharmacompass.com/pdf/news/enforcement-report-week-of-february-22-2023-51785.pdf

FDA
22 Feb 2023

https://www.fiercepharma.com/pharma/merck-telegraphs-closure-pa-antibiotics-plant-employs-300

F. Kansteiner FIERCEPHARMA
25 Mar 2022

http://www.pharmatimes.com/news/novel_antibiotic_recarbrio_has_launched_in_the_uk_1357341

PHARMATIMES
20 Nov 2020

https://investors.merck.com/news/press-release-details/2020/FDA-Approves-Mercks-RECARBRIO-imipenem-cilastatin-and-relebactam-for-the-Treatment-of-Adults-with-Hospital-Acquired-and-Ventilator-Associated-Bacterial-Pneumonia-HABPVABP/default.aspx

MERCK
05 Jun 2020

https://www.businesswire.com/news/home/20200506005158/en

BUSINESSWIRE
06 May 2020

https://www.businesswire.com/news/home/20200506005158/en/Results-Phase-3-Trial-Evaluating-Efficacy-Safety

BUSINESSWIRE
05 May 2020

https://www.ema.europa.eu/en/news/meeting-highlights-committee-medicinal-products-human-use-chmp-9-12-december-2019

EMA
14 Dec 2019

https://www.fiercepharma.com/marketing/aiming-for-label-expansion-merck-touts-new-trial-results-for-antibiotic-recarbrio

E. Sagonowsky FIERCE PHARMA
03 Oct 2019

https://www.biospace.com/article/merck-s-recarbrio-shows-success-in-late-stage-trial-for-habp-vabp-patients/

Alex Keown BIOSPACE
30 Sep 2019

https://endpts.com/merck-touts-phase-iii-data-for-antibacterial-recarbrio-sanofi-to-ax-200-jobs-in-japan-report/

Kathy Wong ENDPTS
30 Sep 2019

https://www.fiercepharma.com/pharma/as-officials-grapple-antimicrobial-resistance-merck-scores-fda-approval-for-new

Eric Sagonowsky FIERCE PHARMA
17 Jul 2019

https://in.reuters.com/article/us-merck-co-fda/mercks-treatment-for-urinary-abdominal-infections-gets-fda-approval-idINKCN1UC19W

REUTERS
17 Jul 2019

https://www.biospace.com/article/fda-action-alert-karyopharm-merck-and-celgene/

Mark Terry BIOSPACE
01 Jul 2019

https://www.fiercepharma.com/pharma/merck-scores-zerbaxa-label-expansion-years-after-cubist-buyout

Eric Sagonowsky FIERCE PHARMA
05 Jun 2019

http://www.pharmatimes.com/news/fda_accepts_two_of_msds_new_drug_applications_1277462

Anna Smith PHARMA TIMES
06 Feb 2019

https://www.pharmacompass.com/pdf/news/hospira-healthcare-india-pvt-ltd-on-fda-import-alert-list-1549480434.pdf

FDA
01 Aug 2018

http://www.prnewswire.com/news-releases/shionogi-announces-positive-top-line-results-for-cefiderocol-pivotal-cuti-clinical-trial-300389912.html

PR NEWSWIRE
12 Jan 2017

https://www.pharmacompass.com/pdf/news/hospira-healthcare-india-private-limited-fails-edqm-inspection-1471672382.pdf

EDQM
18 Aug 2016

http://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=D-0346-2015&w=01282015&lang=eng

FDA
28 Jan 2015
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