Suppliers / Laboratorio Lkm

Laboratorio Lkm

Argentina Updated 9 July 2026

Laboratorio Lkm is a finished-dose manufacturer based in Argentina. It appears in 102 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with ANMAT (AR), ARCSA (EC) and ISP (CL). Its GMP standing is certified by INVIMA (CO). Customs aggregates show $7.2M of exports covering 285 molecules to 7 destinations in 2023.

0
active US DMFs
0
valid CEPs
3
registered plants
102
filings across 5 regulators

Registered plants

Site FDA FEI
BUENOS AIRES, Argentina Not on file
Argentina, Colombia Not on file
Buenos Aires, Colombia Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ANMAT (AR) 55 None
ARCSA (EC) 36 None
ISP (CL) 6 None
MINSA (CR) 4 None
INVIMA (CO) 1 2

Scale

Year Revenue Exports Destinations
2023 Not reported $7.2M 7
2022 Not reported $6.2M 7

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 We do not publish the identity of any buyer.

Questions about Laboratorio Lkm

Does Laboratorio Lkm hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorio Lkm. It does have 102 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratorio Lkm manufacture?
3 registered sites are on record, in Argentina and Colombia (Buenos Aires, Argentina and Buenos Aires). Every site is listed on this page with the register it came from.
Which regulators recognise Laboratorio Lkm'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.

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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
EudraGMDP and national regulators
GMP certificates
Customs aggregates
Export values, molecule and destination counts