HERBRAND PharmaChemicals GmbH

Gengenbach, GermanyFEI 3003310388API manufacture registered

HERBRAND PharmaChemicals GmbH is a drug establishment in Gengenbach, Germany, registered with the US FDA under FEI 3003310388. Its registered operations are: API manufacture. 24 EU/UK GMP certificates are matched to this site, 12 inspected within the last three years.

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.

API manufacture

GMP documents matched to this site (24)

DocumentAuthorityInspectionSource
DE_BW_01_GMP_2026_0136
GMP certificate
Competent authority of Germany23 Apr 2026
within 3-year review window
EudraGMDP
DE_BW_01_GMP_2026_0144
GMP certificate
Competent authority of Germany23 Apr 2026
within 3-year review window
EudraGMDP
DE_BW_01_GMP_2026_0140
GMP certificate
Competent authority of Germany23 Apr 2026
within 3-year review window
EudraGMDP
DE_BW_01_GMP_2026_0141
GMP certificate
Competent authority of Germany23 Apr 2026
within 3-year review window
EudraGMDP
DE_BW_01_GMP_2026_0143
GMP certificate
Competent authority of Germany23 Apr 2026
within 3-year review window
EudraGMDP
DE_BW_01_GMP_2026_0142
GMP certificate
Competent authority of Germany23 Apr 2026
within 3-year review window
EudraGMDP
DE_BW_01_GMP_2026_0145
GMP certificate
Competent authority of Germany23 Apr 2026
within 3-year review window
EudraGMDP
DE_BW_01_GMP_2026_0138
GMP certificate
Competent authority of Germany23 Apr 2026
within 3-year review window
EudraGMDP
DE_BW_01_GMP_2026_0137
GMP certificate
Competent authority of Germany23 Apr 2026
within 3-year review window
EudraGMDP
DE_BW_01_GMP_2026_0147
GMP certificate
Competent authority of Germany23 Apr 2026
within 3-year review window
EudraGMDP
DE_BW_01_GMP_2026_0146
GMP certificate
Competent authority of Germany23 Apr 2026
within 3-year review window
EudraGMDP
DE_BW_01_GMP_2026_0139
GMP certificate
Competent authority of Germany23 Apr 2026
within 3-year review window
EudraGMDP
DE_BW_01_GMP_2023_0174
GMP certificate
Competent authority of Germany25 Jun 2023
outside 3-year review window
EudraGMDP
DE_BW_01_GMP_2023_0172
GMP certificate
Competent authority of Germany26 May 2023
outside 3-year review window
EudraGMDP
DE_BW_01_GMP_2023_0171
GMP certificate
Competent authority of Germany26 May 2023
outside 3-year review window
EudraGMDP
DE_BW_01_GMP_2023_0169
GMP certificate
Competent authority of Germany26 May 2023
outside 3-year review window
EudraGMDP
DE_BW_01_GMP_2023_0175
GMP certificate
Competent authority of Germany26 May 2023
outside 3-year review window
EudraGMDP
DE_BW_01_GMP_2023_0173
GMP certificate
Competent authority of Germany26 May 2023
outside 3-year review window
EudraGMDP
DE_BW_01_GMP_2023_0168
GMP certificate
Competent authority of Germany26 May 2023
outside 3-year review window
EudraGMDP
DE_BW_01_GMP_2023_0170
GMP certificate
Competent authority of Germany26 May 2023
outside 3-year review window
EudraGMDP
DE_BW_01_GMP_2023_0163
GMP certificate
Competent authority of Germany26 May 2023
outside 3-year review window
EudraGMDP
DE_BW_01_GMP_2023_0164
GMP certificate
Competent authority of Germany26 May 2023
outside 3-year review window
EudraGMDP
DE_BW_01_GMP_2023_0166
GMP certificate
Competent authority of Germany26 May 2023
outside 3-year review window
EudraGMDP
DE_BW_01_GMP_2023_0165
GMP certificate
Competent authority of Germany26 May 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.