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  • TABLET;ORAL - 0.125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL - 0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL - 0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL - 0.75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL - 1.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL - 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=213444

FDA
03 Feb 2022

https://www.fiercebiotech.com/biotech/chase-after-selling-last-biotech-to-allergan-gets-cash-to-start-pivotal-trials-depression

Nick Paul Taylor FIERCEBIOTECH
20 Oct 2021

https://www.pharmacompass.com/pdf/news/enforcement-report-week-of-september-18-2019-1568770223.pdf

FDA
18 Sep 2019

https://www.fiercepharma.com/pharma/public-citizen-says-enough-enough-dopamine-agonist-petition-files-for-injunction

Kyle Blankenship FIERCE PHARMA
01 May 2019

https://www.thehindubusinessline.com/companies/alembic-pharma-gets-usfda-nod-for-parkinsons-treatment-drug/article25897238.ece

HINDU BUSINESS LINE
03 Jan 2019

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=204518

FDA
02 Jan 2019

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=207011

FDA
19 Dec 2018

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=211088

FDA
09 Oct 2018

https://www.pharmacompass.com/pdf/news/enforcement-report-week-of-september-19-2018-1537361296.pdf

FDA
19 Sep 2018

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=202891

FDA
16 Dec 2017

https://economictimes.indiatimes.com/industry/healthcare/biotech/pharmaceuticals/cadila-gets-usfda-nod-for-generic-drug-to-treat-parkinsons/articleshow/62069179.cms

ECONOMIC TIMES
14 Dec 2017

http://www.fiercebiotech.com/venture-capital/pharma-two-b-raises-30m-for-parkinson-s-phase-3-from-biogen-backed-fund-adds-ex

Nick Paul Taylor FIERCE BIOTECH
28 Feb 2017

https://www.pharmacompass.com/pdf/news/actavis-elizabeths-generics-pramipexole-dihydrochloride-approved-in-us-1477132960.pdf

FDA
19 Oct 2016

https://www.pharmacompass.com/pdf/news/macleods-receives-fda-approval-for-generic-pramipexole-dihydrchloride-1467204473.pdf

FDA
24 Jun 2016

http://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=D-0653-2016&w=02172016&lang=eng

FDA
17 Feb 2016

http://www.reuters.com/article/usa-court-ftc-boehringer-idUSL2N14Y2Z7

Diane Bartz REUTERS
20 Jan 2016

http://economictimes.indiatimes.com/industry/healthcare/biotech/pharmaceuticals/dr-reddys-laboratories-launches-generic-drug-for-parkinsons-treatment-in-us/articleshow/48456433.cms

PTI THE ECONOMIC TIMES
12 Aug 2015

http://www.fdalawblog.net/fda_law_blog_hyman_phelps/2015/02/fda-draft-guidance-on-disclosing-risk-information-discourages-companies-from-meeting-current-regulat.html

Dara Katcher Levy FDA LAW BLOG
16 Feb 2015

http://www.bloomberg.com/news/2014-12-09/malaria-2014-deaths-may-top-20-000-in-ebola-hit-nations.html

Press Release Bloomberg
09 Dec 2014
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