Epic Pharma
United States 139 employees Updated 9 July 2026
Epic Pharma is a finished-dose manufacturer based in United States. It appears in 335 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with US FDA and DMP (NO). Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 7 December 2023 as NAI.
2
registered plants
2 with an FDA FEI number
335
filings
across 2 regulators
These figures were checked against the regulators' own files on 25 July 2026
Inspections
8 of 8 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.
Inspection history
- 7 December 2023 NAI US FDA
- 23 October 2023 VAI US FDA
- 1 February 2019 VAI US FDA
- 6 November 2018 VAI US FDA
- 21 April 2017 VAI US FDA
- 4 June 2015 VAI US FDA
- 23 December 2013 NAI US FDA
- 1 November 2012 NAI US FDA
NAI means no action indicated, VAI means voluntary action indicated, and OAI means
official action indicated.
Registered plants
| Site | FDA FEI |
| Westbury, United States | 3031887837 |
| Laurelton, United States | 2431929 |
Filings and GMP by regulator
| Regulator | Filings | GMP certificates |
| US FDA | 329 | 1 |
| DMP (NO) | 6 | None |
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Open risk flags
- 43 active litigation matters are on record.
- The most recent inspection outcome was NAI, on 7 December 2023.
Sources on this page
- FDA
- Drug master files, establishment registration, inspection classifications
- EDQM
- Certificates of suitability
- EudraGMDP and national regulators
- GMP certificates