Suppliers / Apozeal Pharmaceuticals

Apozeal Pharmaceuticals

United States Updated 9 July 2026

Apozeal Pharmaceuticals is a finished-dose manufacturer based in United States. It appears in 7 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its most recent recorded inspection, by US FDA, closed on 15 October 2025 as OAI.

0
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
7
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
7 of 7 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 15 October 2025 OAI US FDA
  • 15 December 2021 NAI US FDA
  • 9 April 2019 OAI US FDA
  • 9 November 2018 NAI US FDA
  • 5 April 2017 NAI US FDA
  • 21 November 2012 VAI US FDA
  • 27 October 2009 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Levittown, United States 3004536846

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA 7 None

Questions about Apozeal Pharmaceuticals

Does Apozeal Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Apozeal Pharmaceuticals. It does have 7 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Is Apozeal Pharmaceuticals FDA-registered?
One site operated by Apozeal Pharmaceuticals carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Apozeal Pharmaceuticals's last inspection go?
The most recent inspection on record closed on 15 October 2025 as OAI (Official Action Indicated, the worst classification: objectionable conditions were found and regulatory action was warranted). 7 inspections are on file, of which 2 closed as OAI.
Where does Apozeal Pharmaceuticals manufacture?
1 registered site is on record, in United States (Levittown). Every site is listed on this page with the register it came from.
Where does Apozeal Pharmaceuticals file?
Filings are on record with US FDA, 7 in total.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Open risk flags

  • The most recent inspection outcome was OAI, on 15 October 2025.

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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability