Suppliers / Laboratorios Fabra S A

Laboratorios Fabra S A

Argentina Updated 9 July 2026

Laboratorios Fabra S A is a finished-dose manufacturer based in Argentina. It appears in 110 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with ANMAT (AR), ARCSA (EC) and MINSA (CR).

0
active US DMFs
0
valid CEPs
0
registered plants
110
filings across 4 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
ANMAT (AR) 94 None
ARCSA (EC) 7 None
MINSA (CR) 6 None
DIGEMAPS (DO) 3 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 Laboratorios Fabra S A

Does Laboratorios Fabra S A hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorios Fabra S A. It does have 110 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratorios Fabra S A file?
Filings are on record with ANMAT (AR), ARCSA (EC), MINSA (CR) and DIGEMAPS (DO), 110 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