Dynamit Nobel GmbH Explosivstoff- und Systemtechnik

Leverkusen, GermanyFEI 0000001379API manufacture registered

Dynamit Nobel GmbH Explosivstoff- und Systemtechnik is a drug establishment in Leverkusen, Germany, registered with the US FDA under FEI 0000001379. Its registered operations are: Analytical testing, API manufacture. 8 EU/UK GMP certificates are matched to this site.

Sources: FDA Drug Establishments Current Registration Site (checked 2 Nov 2026); EudraGMDP; MHRA GMDP. Methodology

Registered operations

Business operations this establishment declares in its FDA registration. Registration is not an approval and says nothing about EU or UK GMP status.

Analytical testingAPI manufacture

GMP documents matched to this site (8)

DocumentAuthorityInspectionSource
DE_NW_04_GMP_2023_0065
GMP certificate
Competent authority of Germany1 Sept 2023
outside 3-year review window
EudraGMDP
DE_NW_04_GMP_2023_0070
GMP certificate
Competent authority of Germany1 Sept 2023
outside 3-year review window
EudraGMDP
DE_NW_04_GMP_2023_0068
GMP certificate
Competent authority of Germany1 Sept 2023
outside 3-year review window
EudraGMDP
DE_NW_04_GMP_2023_0066
GMP certificate
Competent authority of Germany1 Sept 2023
outside 3-year review window
EudraGMDP
DE_NW_04_GMP_2023_0069
GMP certificate
Competent authority of Germany1 Sept 2023
outside 3-year review window
EudraGMDP
DE_NW_04_GMP_2023_0067
GMP certificate
Competent authority of Germany1 Sept 2023
outside 3-year review window
EudraGMDP
DE_NW_04_GMP_2023_0071
GMP certificate
Competent authority of Germany1 Sept 2023
outside 3-year review window
EudraGMDP
DE_NW_04_GMP_2023_0064
GMP certificate
Competent authority of Germany1 Sept 2023
outside 3-year review window
EudraGMDP

A GMP document is matched to this site when its address names the site's street and its city or postcode. In our latest internal review 59 of 60 sampled matches were the right site (not yet independently reviewed; measured match quality). Check the certificate's own address before relying on it. The three-year review window is the EMA guideline default after an inspection, not an official expiry date.

What this page does not show

  • Which substances are made here: DMFs and CEPs are filed by organisations, not sites, so we do not link substances to this site.
  • Capacity, scale, price or current availability: no regulator publishes these.
  • FDA inspection classifications for this site, which are not yet linked.