Suppliers / Laboratorios Ecar S A

Laboratorios Ecar S A

Colombia Updated 9 July 2026

Laboratorios Ecar S A is a finished-dose manufacturer based in Colombia. It appears in 215 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with INVIMA (CO), ARCSA (EC) and MINSA (CR). Its GMP standing is certified by INVIMA (CO).

0
active US DMFs
0
valid CEPs
2
registered plants
215
filings across 5 regulators

Registered plants

Site FDA FEI
Medellin, Colombia Not on file
Rionegro, Colombia Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
INVIMA (CO) 135 4
ARCSA (EC) 31 None
MINSA (CR) 26 None
DIGEMAPS (DO) 22 None
COFEPRIS (MX) 1 None

Questions about Laboratorios Ecar S A

Does Laboratorios Ecar S A hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorios Ecar S A. It does have 215 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratorios Ecar S A manufacture?
2 registered sites are on record, in Colombia (Medellin and Rionegro). Every site is listed on this page with the register it came from.
Which regulators recognise Laboratorios Ecar S A's GMP?
Current GMP certificates are on record from INVIMA (CO). GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

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.

Comparing suppliers?

Choose your molecules and target markets. Laboratorios Ecar S A comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Comparable suppliers

C.I. Farmacapsulas also in Colombia Laboratorio Profesional also in Colombia Laboratorios Bussie S A also in Colombia Laboratorios Chalver De Colombia, S. A also in Colombia Laboratorios Legrand S A also in Colombia

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
EudraGMDP and national regulators
GMP certificates