Suppliers / Chattem

Chattem

United States Updated 9 July 2026

The public registers hold a second record for Chattem. The fuller profile, with 26 active US DMFs and 1 valid CEPs, is at Chattem Chemicals. Figures on this page cover only this record.

Chattem is a finished-dose manufacturer based in United States. It appears in 13 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with US FDA, ARCSA (EC) and MPA (SE). Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 22 August 2025 as VAI.

0
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
13
filings across 3 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

  • 22 August 2025 VAI US FDA
  • 13 March 2020 VAI US FDA
  • 4 May 2017 NAI US FDA
  • 2 March 2017 NAI US FDA
  • 14 March 2014 NAI US FDA
  • 24 February 2012 NAI US FDA
  • 29 July 2009 NAI US FDA

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

Registered plants

Site FDA FEI
Chattanooga, United States 1022556

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA 10 1
ARCSA (EC) 2 None
MPA (SE) 1 None

Questions about Chattem

Does Chattem hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Chattem. It does have 13 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Chattem FDA-registered?
One site operated by Chattem 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 Chattem's last inspection go?
The most recent inspection on record closed on 22 August 2025 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 7 inspections are on file.
Where does Chattem manufacture?
1 registered site is on record, in United States (Chattanooga). Every site is listed on this page with the register it came from.
Which regulators recognise Chattem's GMP?
Current GMP certificates are on record from US FDA. GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

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 VAI, on 22 August 2025.

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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates