Suppliers / Reckitt Benckiser healthcare (UK)

Reckitt Benckiser healthcare (UK)

Nigeria 2 duplicate records merged Updated 9 July 2026

Reckitt Benckiser healthcare (UK) is a finished-dose manufacturer based in Nigeria. It appears in 1,306 regulatory filings across 38 regulators, without an active US DMF or CEP on file. Its filings concentrate with AIFA (IT), MEDSAFE (NZ) and EMA. Its GMP standing is certified by MHRA (UK), NAFDAC (NG) and ANVISA (Brazil), among 5 authorities. Its most recent recorded inspection, by US FDA, closed on 13 June 2019 as VAI.

0
active US DMFs
0
valid CEPs
12
registered plants
1,306
filings across 38 regulators
These figures were checked against the regulators' own files on 25 July 2026
Inspections
0 of 4 confirmed
Sources: FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 13 June 2019 VAI US FDA
  • 12 October 2018 VAI US FDA
  • 17 August 2017 VAI US FDA
  • 10 May 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
Nottingham, United Arab Emirates Not on file
Hull, United Arab Emirates Not on file
São Paulo, Brazil Not on file
Wallisellen, Switzerland Not on file
HULL, United Kingdom Not on file
NOTTINGHAM, United Kingdom Not on file

6 further sites are on record.

Filings and GMP by regulator

Regulator Filings GMP certificates
AIFA (IT) 232 None
MEDSAFE (NZ) 222 None
EMA 204 None
MHRA (UK) 68 13
FAMHP (BE) 54 None
INFARMED (PT) 54 None
NAFDAC (NG) None 5
ANVISA (Brazil) None 3
CDSCO (India) None 2
DRAP (PK) None 1

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Open risk flags

  • The most recent inspection outcome was VAI, on 13 June 2019.

Sources on this page

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