Suppliers / Laboratorio Eczane Pharma

Laboratorio Eczane Pharma

Argentina Updated 9 July 2026

Laboratorio Eczane Pharma is a finished-dose manufacturer based in Argentina. It appears in 196 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with ARCSA (EC), ANMAT (AR) and MINSA (CR).

0
active US DMFs
0
valid CEPs
0
registered plants
196
filings across 5 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
ARCSA (EC) 96 None
ANMAT (AR) 70 None
MINSA (CR) 24 None
DIGEMAPS (DO) 5 None
RAMA (GE) 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 Laboratorio Eczane Pharma

Does Laboratorio Eczane Pharma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorio Eczane Pharma. It does have 196 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratorio Eczane Pharma file?
Filings are on record with ARCSA (EC), ANMAT (AR), MINSA (CR), DIGEMAPS (DO) and 1 other regulator, 196 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