Suppliers / Basf Grenzach

Basf Grenzach

Germany Updated 9 July 2026

The public registers hold a second record for Basf Grenzach. The fuller profile, with 17 active US DMFs and 14 valid CEPs, is at BASF. Figures on this page cover only this record.

Basf Grenzach is an API manufacturer based in Germany. It holds one active US drug master file. Its GMP standing is certified by ZLG (DE).

1
active US DMFs
0
valid CEPs
1
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Grenzach-Wyhlen, Germany Not on file

What they file, and where

Molecule Regulators Docs
Triclosan US FDA 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
ZLG (DE) None 2

Questions about Basf Grenzach

Does Basf Grenzach hold a US DMF or a CEP?
Basf Grenzach holds 1 active US drug master file. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Where does Basf Grenzach manufacture?
1 registered site is on record, in Germany (Grenzach-wyhlen). Every site is listed on this page with the register it came from.
What does Basf Grenzach make?
1 molecule is on record against Basf Grenzach, including Triclosan. Each links through to that molecule's full manufacturer list.
Which regulators recognise Basf Grenzach's GMP?
Current GMP certificates are on record from ZLG (DE). GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Sources on this page

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