Suppliers / Mpp Pharma

Mpp Pharma

United States Updated 9 July 2026

Mpp Pharma is a finished-dose manufacturer based in United States. It appears in 23 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 20 September 2024 as VAI.

0
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
23
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
8 of 8 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 20 September 2024 VAI US FDA
  • 13 September 2024 VAI US FDA
  • 21 April 2021 VAI US FDA
  • 4 April 2016 NAI US FDA
  • 19 February 2014 VAI US FDA
  • 30 January 2013 VAI US FDA
  • 5 November 2010 VAI US FDA
  • 1 December 2009 OAI US FDA

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

Registered plants

Site FDA FEI
Kansas City, United States 1930436

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA 23 1

Questions about Mpp Pharma

Does Mpp Pharma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Mpp Pharma. It does have 23 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Is Mpp Pharma FDA-registered?
One site operated by Mpp Pharma 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 Mpp Pharma's last inspection go?
The most recent inspection on record closed on 20 September 2024 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 8 inspections are on file, of which 1 closed as OAI.
Where does Mpp Pharma manufacture?
1 registered site is on record, in United States (Kansas City). Every site is listed on this page with the register it came from.
Which regulators recognise Mpp Pharma'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

  • 1 active litigation matter is on record.
  • The most recent inspection outcome was VAI, on 20 September 2024.

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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

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