Suppliers / Reckitt Benckiser Healthcare Manufacturing (Thailand)

Reckitt Benckiser Healthcare Manufacturing (Thailand)

Thailand 2 duplicate records merged Updated 9 July 2026

Reckitt Benckiser Healthcare Manufacturing (Thailand) is a finished-dose manufacturer based in Thailand. It appears in 45 regulatory filings across 7 regulators, without an active US DMF or CEP on file. Its filings concentrate with NPRA (MY), EDE (AE) and NAFDAC (NG). Its GMP standing is certified by ANVISA (Brazil), US FDA and MHRA (UK), among 5 authorities. Its most recent recorded inspection, by US FDA, closed on 8 September 2023 as VAI.

0
active US DMFs
0
valid CEPs
5
registered plants 1 with an FDA FEI number
45
filings across 7 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
3 of 3 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Inspection history

  • 8 September 2023 VAI US FDA
  • 20 October 2017 NAI US FDA
  • 9 September 2016 VAI US FDA

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

Registered plants

Site FDA FEI
Samut Prakan, United Arab Emirates Not on file
SAMUTPRAKARN, Thailand Not on file
BANG PHLI (BANGPLEE), Thailand Not on file
Samut Prakan, Thailand Not on file
Thailand, Thailand 3008264702

Filings and GMP by regulator

Regulator Filings GMP certificates
NPRA (MY) 19 None
EDE (AE) 10 None
NAFDAC (NG) 5 1
DAV (Vietnam) 4 None
BOMRA (BW) 3 None
MINSA (CR) 3 None
ANVISA (Brazil) None 1
US FDA None 1
MHRA (UK) None 1
EMA None 1

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Open risk flags

  • The most recent inspection outcome was VAI, on 8 September 2023.

Sources on this page

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