Suppliers / Novo Nordisk A/S

Novo Nordisk A/S

Denmark NVO Updated 9 July 2026

Novo Nordisk A/S is a finished-dose manufacturer based in Denmark. It appears in 2,748 regulatory filings across 41 regulators, without an active US DMF or CEP on file. Its filings concentrate with AIFA (IT), FAMHP (BE) and MHRA (UK). Its GMP standing is certified by ANVISA (Brazil), NCELS (KZ) and NAFDAC (NG), among 4 authorities. Its most recent recorded inspection, by US FDA, closed on 4 May 2023 as VAI. Customs aggregates show $21K of exports covering 3,719 molecules to 8 destinations in 2025.

0
active US DMFs
0
valid CEPs
12
registered plants 2 with an FDA FEI number
2,748
filings across 41 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
2 of 2 confirmed
Inspections
8 of 8 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

  • 4 May 2023 VAI US FDA
  • 29 March 2023 VAI US FDA
  • 2 December 2022 VAI US FDA
  • 5 December 2019 VAI US FDA
  • 6 September 2019 NAI US FDA
  • 18 May 2018 NAI US FDA
  • 29 August 2017 NAI US FDA
  • 8 February 2017 VAI US FDA

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

Registered plants

Site FDA FEI
Bagsvaerd, United Arab Emirates Not on file
Bagsvaerd, United Arab Emirates Not on file
Gentofte, United Arab Emirates Not on file
Hjoerring, United Arab Emirates Not on file
MALØV, Denmark Not on file
Bagsvaerd, Denmark Not on file

6 further sites are on record.

Filings and GMP by regulator

Regulator Filings GMP certificates
AIFA (IT) 356 None
FAMHP (BE) 323 None
MHRA (UK) 299 None
Health Canada 250 None
EMA 209 1
INFARMED (PT) 203 None
ANVISA (Brazil) None 9
NCELS (KZ) None 4
NAFDAC (NG) None 2

Scale

Year Revenue Exports Destinations
2025 Not reported $21K 8
2024 Not reported $25K 7
2023 $610.0B $24K 7
2022 $500.0B $2K 4
2021 $380.0B Not reported Not reported

Export figures are customs aggregates. We do not publish the identity of any buyer.

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Open risk flags

  • 100 active litigation matters are on record.
  • 2 recent serious compliance events are on record.
  • The most recent inspection outcome was VAI, on 4 May 2023.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates
Customs aggregates
Export values, molecule and destination counts
Company filings
Revenue as reported