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  • TABLET;ORAL - 25MG;25MG
  • TABLET;ORAL - 50MG;50MG
  • CAPSULE;ORAL - 25MG;37.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL - 25MG;37.5MG
  • TABLET;ORAL - 50MG;75MG
  • TABLET;ORAL - 10MG;25MG
  • TABLET;ORAL - 5MG;12.5MG
  • TABLET;ORAL - 12.5MG;10MG
  • TABLET;ORAL - 12.5MG;20MG
  • TABLET;ORAL - 25MG;20MG
  • TABLET;ORAL - 12.5MG;100MG
  • TABLET;ORAL - 12.5MG;50MG
  • TABLET;ORAL - 25MG;100MG
  • CAPSULE;ORAL - 12.5MG
  • TABLET;ORAL - 12.5MG;150MG
  • TABLET;ORAL - 12.5MG;300MG
  • TABLET;ORAL - 12.5MG;75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL - 25MG;300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL - 12.5MG;160MG
  • TABLET;ORAL - 12.5MG;320MG
  • TABLET;ORAL - 12.5MG;80MG
  • TABLET;ORAL - 25MG;160MG
  • TABLET;ORAL - 25MG;320MG
  • TABLET;ORAL - 16MG;12.5MG
  • TABLET;ORAL - 32MG;12.5MG
  • TABLET;ORAL - 32MG;25MG
  • TABLET;ORAL - 12.5MG;40MG
  • TABLET;ORAL - 12.5MG;80MG
  • TABLET;ORAL - 25MG;80MG
  • TABLET;ORAL - 12.5MG;20MG
  • TABLET;ORAL - 12.5MG;40MG
  • TABLET;ORAL - 25MG;40MG
  • TABLET, EXTENDED RELEASE;ORAL - 12.5MG;EQ 100MG TARTRATE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET, EXTENDED RELEASE;ORAL - 12.5MG;EQ 25MG TARTRATE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET, EXTENDED RELEASE;ORAL - 12.5MG;EQ 50MG TARTRATE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL - EQ 150MG BASE;12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL - EQ 150MG BASE;25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL - EQ 300MG BASE;12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL - EQ 300MG BASE;25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL - EQ 10MG BASE;12.5MG;160MG
  • TABLET;ORAL - EQ 10MG BASE;25MG;160MG
  • TABLET;ORAL - EQ 10MG BASE;25MG;320MG
  • TABLET;ORAL - EQ 5MG BASE;12.5MG;160MG
  • TABLET;ORAL - EQ 5MG BASE;25MG;160MG
  • TABLET;ORAL - 25MG
  • TABLET;ORAL - 50MG

https://www.pharmacompass.com/pdf/news/enforcement-report-week-of-november-8-2023-82126.pdf

FDA
08 Nov 2023

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=204382

FDA
11 Aug 2023

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=204801

FDA
01 Jun 2023

https://www.pharmacompass.com/pdf/news/enforcement-report-week-of-january-25-2023-68767.pdf

FDA
25 Jan 2023

https://health.economictimes.indiatimes.com/news/pharma/zydus-lifesciences-gets-usfda-nod-for-generic-hypertension-drug/95374653

HEALTH ET
08 Nov 2022

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=215666

FDA
04 Nov 2022

https://www.pharmacompass.com/pdf/news/enforcement-report-week-of-november-2-2022-77418.pdf

FDA
02 Nov 2022

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/aurobindo-pharma-usa-inc-initiates-voluntary-nationwide-recall-two-2-lots-quinapril-and

FDA
26 Oct 2022

https://www.pharmacompass.com/pdf/news/enforcement-report-week-of-august-17-2022-1660735823.pdf

FDA
17 Aug 2022

https://www.pharmacompass.com/pdf/news/enforcement-report-week-of-april-13-2022-1649826529.pdf

FDA
13 Apr 2022

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/pfizer-voluntary-nationwide-recall-lots-accuretictm-quinapril-hclhydrochlorothiazide-quinapril-and

FDA
23 Mar 2022

https://recalls-rappels.canada.ca/en/alert-recall/pfizer-recalls-accuretic-blood-pressure-tablets-due-nitrosamine-impurity

HEALTH CANADA
05 Mar 2022

http://www.pharmabiz.com/NewsDetails.aspx?aid=145442&sid=2

PHARMABIZ
27 Jan 2022

https://www.pharmacompass.com/pdf/news/enforcement-report-week-of-december-22-2021-1640158210.pdf

FDA
22 Dec 2021

http://www.koreabiomed.com/news/articleView.html?idxno=12631

Shim Hyun-tai KOREABIOMED
24 Nov 2021

https://www.pharmacompass.com/pdf/news/enforcement-report-week-of-november-11-2021-1636538960.pdf

FDA
10 Nov 2021

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=215562

FDA
03 Nov 2021

https://www.fda.gov/drugs/drug-safety-and-availability/fda-approves-label-changes-hydrochlorothiazide-describe-small-risk-non-melanoma-skin-cancer#:~:text=The%20increased%20risk%20of%20developing,squamous%20cell%20carcinoma%20(SCC).

CISION
24 Aug 2020

https://www.fda.gov/drugs/drug-safety-and-availability/fda-approves-label-changes-hydrochlorothiazide-describe-small-risk-non-melanoma-skin-cancer#:~:text=%5B8%2F20%2F2020%5D,HCTZ%20use%20and%20to%20encourage

FDA
20 Aug 2020

https://www.pharmaexcipients.com/news/polyvinyl-acetate-odt/

PHARMAEXCIPIENTS
19 Aug 2020

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=212678

FDA
16 Jul 2020

https://www.fiercepharma.com/pharma/astrazeneca-hawks-suite-hyptertension-drugs-for-350m-latest-asset-sale

K. Blankenship FIERCE PHARMA
03 Mar 2020

https://www.fiercepharma.com/manufacturing/fda-warning-letter-tags-torrent-as-key-offender-production-tainted-blood-pressure

Eric Palmer FIERCE PHARMA
17 Oct 2019

https://www.pharmacompass.com/pdf/news/torrent-pharmaceuticals-limited-expands-voluntary-nationwide-recall-of-losartan-potassium-tablets-1569033044.pdf

FDA
21 Sep 2019

https://www.indiainfoline.com/article/news-top-story/glenmark-pharma-terms-report-on-stake-sale-to-premjiinvest-speculative-119082600070_1.html

INDIAINFOLINE
27 Aug 2019

https://economictimes.indiatimes.com/industry/healthcare/biotech/pharmaceuticals/glenmark-recalls-products-from-us-market/articleshow/70826067.cms

ECONOMICTIMES
26 Aug 2019

https://www.pharmacompass.com/pdf/news/enforcement-report-week-of-august-21-2019-1566366765.pdf

FDA
21 Aug 2019

https://www.accessdata.fda.gov/scripts/ires/index.cfm?action=print.getPrintData&ts=6312019105346

FDA
31 Jul 2019

https://www.bloomberg.com/news/articles/2019-06-18/fourth-carcinogen-discovered-in-heart-pills-used-by-millions

BLOOMBERG
19 Jun 2019

https://www.pharmacompass.com/pdf/news/enforcement-report-week-of-may-8-2019-1557294096.pdf

FDA
08 May 2019

http://pharmabiz.com/ArticleDetails.aspx?aid=115527&sid=1

PHARMABIZ
06 May 2019

https://www.raps.org/news-and-articles/news-articles/2019/4/ema-urges-pioglitazone-manufacturers-to-check-for

Zachary Brennan RAPS
26 Apr 2019

https://www.pharmacompass.com/pdf/news/updated-torrent-pharmaceuticals-limited-expands-voluntary-nationwide-recall-of-losartan-potassium-tablets-1555650822.pdf

FDA
19 Apr 2019

https://www.pharmacompass.com/pdf/news/enforcement-report-week-of-march-27-2019-1553661457.pdf

FDA
27 Mar 2019

https://www.raps.org/news-and-articles/news-articles/2019/3/to-prevent-losartan-shortages-fda-allows-higher-i

Zachary Brennan RAPS
22 Mar 2019

https://www.fda.gov/Drugs/DrugSafety/ucm613916.htm

FDA
20 Mar 2019

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=202544

FDA
06 Mar 2019

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=205769

FDA
06 Mar 2019

https://www.pharmacompass.com/pdf/news/health-canada-issues-recall-of-teva-canadas-teva-losartan-hctz-50125mg-tablet-1552626132.pdf

FDA
06 Mar 2019

https://www.pharmacompass.com/pdf/news/macleods-pharmaceuticals-issues-voluntary-nationwide-consumer-level-recall-of-one-lot-blm-715a-of-losartan-potassiumhydrochlorothiazide-combination-tablets-100mg25mg-1551155408.pdf

FDA
26 Feb 2019

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=208358

FDA
11 Feb 2019

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=209281

FDA
07 Feb 2019

https://www.pharmacompass.com/pdf/news/enforcement-report-week-of-february-6-2019-1549474146.pdf

FDA
06 Feb 2019

https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2019/68976a-eng.php

HEALTH CANADA
03 Feb 2019

https://www.fda.gov/Drugs/DrugSafety/ucm613916.htm?utm_campaign=UPDATE%20on%20angiotensin%20II%20receptor%20blocker%20%28ARB%29%20recalls%3A%20Torrent%20further%20expands&utm_medium=email&utm_source=Eloqua

FDA
23 Jan 2019

https://www.fda.gov/downloads/Drugs/DrugSafety/UCM628993.pdf?utm_campaign=UPDATE%20on%20angiotensin%20II%20receptor%20blocker%20%28ARB%29%20recalls%3A%20Torrent%20further%20expands&utm_medium=email&utm_source=Eloqua

FDA
23 Jan 2019

https://www.pharmacompass.com/pdf/news/torrent-pharmaceuticals-recalls-losartan-potassium-and-losartanhctz-tablets-1548327958.pdf

FDA
23 Jan 2019

https://www.pharmacompass.com/pdf/news/enforcement-report-week-of-january-23-2019-1548227584.pdf

FDA
23 Jan 2019
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