Teva

Israel Updated 9 July 2026

The public registers hold a second record for Teva. The fuller profile, with 22 active US DMFs and 2 valid CEPs, is at Teva. Figures on this page cover only this record.

Teva is a finished-dose manufacturer based in Israel. It appears in 3,528 regulatory filings across 7 regulators, without an active US DMF or CEP on file. Its filings concentrate with AIFA (IT), FAMHP (BE) and MPA (SE).

active US DMFs

valid CEPs

registered plants

3,528

filings across 7 regulators

Filings and GMP by regulator

Regulator	Filings	GMP certificates
AIFA (IT)	2,130	None
FAMHP (BE)	617	None
MPA (SE)	321	None
INFARMED (PT)	272	None
DMP (NO)	89	None
URPL (PL)	52	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 Teva

Does Teva hold a US DMF or a CEP?

No active US drug master file or valid CEP is on record for Teva. It does have 3,528 filings with 7 regulators, so it is registered, just not with the two strong registers buyers usually screen on.

Where does Teva file?

Filings are on record with AIFA (IT), FAMHP (BE), MPA (SE), INFARMED (PT) and 3 other regulators, 3,528 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

Abic also in Israel Dexcel Pharma also in Israel Padagis Israel also in Israel Rafa Laboratories also in Israel Taro Pharmaceuticals also in Israel

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