Suppliers / Laboratorio Pablo Cassará

Laboratorio Pablo Cassará

Argentina 2 duplicate records merged Updated 9 July 2026

Laboratorio Pablo Cassará is a finished-dose manufacturer based in Argentina. It appears in 450 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO), ANMAT (AR) and ARCSA (EC). Customs aggregates show $10.1M of exports covering 650 molecules to 17 destinations in 2023.

0
active US DMFs
0
valid CEPs
2
registered plants
450
filings across 5 regulators

Registered plants

Site FDA FEI
BUENOS AIRES, Argentina Not on file
BUENOS AIRES, Argentina Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 285 None
ANMAT (AR) 111 None
ARCSA (EC) 36 None
MINSA (CR) 14 None
RAMA (GE) 4 None

Scale

Year Revenue Exports Destinations
2023 Not reported $10.1M 17
2022 Not reported $9.9M 16

Export figures are customs aggregates. We do not publish the identity of any buyer.

Questions about Laboratorio Pablo Cassará

Does Laboratorio Pablo Cassará hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorio Pablo Cassará. It does have 450 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratorio Pablo Cassará manufacture?
2 registered sites are on record, in Argentina (Buenos Aires among others). Every site is listed on this page with the register it came from.
Where does Laboratorio Pablo Cassará file?
Filings are on record with DIGEMAPS (DO), ANMAT (AR), ARCSA (EC), MINSA (CR) and 1 other regulator, 450 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

Abbott Laboratories Argentina also in Argentina Amarin Technologies also in Argentina Eriochem also in Argentina Glenmark Generics also in Argentina Gobbi Novag also in Argentina

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
Customs aggregates
Export values, molecule and destination counts