Suppliers / Centurion

Centurion

India 4 employees Updated 9 July 2026

Centurion is a finished-dose manufacturer based in India. It appears in 13 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with NMRC (NA), JFDA (JO) and TITCK (TR).

0
active US DMFs
0
valid CEPs
0
registered plants
13
filings across 4 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
NMRC (NA) 7 None
JFDA (JO) 2 None
TITCK (TR) 2 None
EEC_EAEU 2 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 Centurion

Does Centurion hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Centurion. It does have 13 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Centurion file?
Filings are on record with NMRC (NA), JFDA (JO), TITCK (TR) and EEC (Eurasian Economic Union), 13 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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Sources on this page

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