Suppliers / TEVA

TEVA

Israel 4 duplicate records merged Updated 9 July 2026

TEVA is a finished-dose manufacturer based in Israel. It appears in 982 regulatory filings across 8 regulators, without an active US DMF or CEP on file. Its filings concentrate with FAMHP (BE), EMA and AIFA (IT).

0
active US DMFs
0
valid CEPs
0
registered plants
982
filings across 8 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
FAMHP (BE) 417 None
EMA 222 None
AIFA (IT) 122 None
MPA (SE) 114 None
DMP (NO) 66 None
INFARMED (PT) 37 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.

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Sources on this page

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