Suppliers / Bayer Schering Pharma

Bayer Schering Pharma

Germany Updated 9 July 2026

Bayer Schering Pharma is an API manufacturer based in Germany. It appears in 33 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with MPA (SE), EMA and NAFDAC (NG).

0
active US DMFs
0
valid CEPs
0
registered plants
33
filings across 3 regulators

What they file, and where

Molecule Regulators Docs
Vardenafil SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Vardenafil API

Filings and GMP by regulator

Regulator Filings GMP certificates
MPA (SE) 17 None
EMA 13 None
NAFDAC (NG) 3 None

Questions about Bayer Schering Pharma

Does Bayer Schering Pharma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Bayer Schering Pharma. It does have 33 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
What does Bayer Schering Pharma make?
1 molecule is on record against Bayer Schering Pharma, including Vardenafil. Each links through to that molecule's full manufacturer list.
Where does Bayer Schering Pharma file?
Filings are on record with MPA (SE), EMA and NAFDAC (NG), 33 in total.

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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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability