Suppliers / Kenwell Ab, Suecia

Kenwell Ab, Suecia

Sweden Updated 9 July 2026

Kenwell Ab, Suecia is a finished-dose manufacturer based in Sweden. It appears in 1 regulatory filing across 1 regulator, without an active US DMF or CEP on file.

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

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 1 None

Limited public record

Beyond the filing counts above, the public registers hold no plant, inspection or portfolio detail for this company as at 9 July 2026. We report that as a gap rather than inferring an answer.

Questions about Kenwell Ab, Suecia

Does Kenwell Ab, Suecia hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Kenwell Ab, Suecia. It does have 1 filing with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Kenwell Ab, Suecia file?
Filings are on record with DIGEMAPS (DO), 1 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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Comparable suppliers

Galenica AB also in Sweden Mcneil Ab also in Sweden Qpharma Ab also in Sweden Sever Pharma Solutions AB also in Sweden Chemoswed Ab also in Sweden

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