Suppliers / Laboratorios Zeyco, S.A. de C.V

Laboratorios Zeyco, S.A. de C.V

Mexico Updated 9 July 2026

Laboratorios Zeyco, S.A. de C.V is a finished-dose manufacturer based in Mexico. It appears in 26 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO), MINSA (CR) and ARCSA (EC). Its GMP standing is certified by MFDS (Korea), COFEPRIS (MX) and US FDA. Its most recent recorded inspection, by US FDA, closed on 10 November 2023 as NAI. Customs aggregates show $37K of exports covering 2 molecules to 2 destinations in 2024.

0
active US DMFs
0
valid CEPs
3
registered plants 1 with an FDA FEI number
26
filings across 6 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 10 November 2023 NAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Zapopan, United Arab Emirates Not on file
Zapopan, Mexico Not on file
Mexico, Mexico 3004109292

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 7 None
MINSA (CR) 6 None
ARCSA (EC) 5 None
RAMA (GE) 4 None
EDE (AE) 3 None
EEC_EAEU 1 None
MFDS (Korea) None 2
COFEPRIS (MX) None 2
US FDA None 1

Scale

Year Revenue Exports Destinations
2024 Not reported $37K 2
2023 Not reported $2.1M 19
2022 Not reported $2.2M 21

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 We do not publish the identity of any buyer.

Questions about Laboratorios Zeyco, S.A. de C.V

Does Laboratorios Zeyco, S.A. de C.V hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorios Zeyco, S.A. de C.V. It does have 26 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Laboratorios Zeyco, S.A. de C.V FDA-registered?
One site operated by Laboratorios Zeyco, S.A. de C.V carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Laboratorios Zeyco, S.A. de C.V's last inspection go?
The most recent inspection on record closed on 10 November 2023 as NAI (No Action Indicated: nothing objectionable was found). 1 inspection is on file.
Where does Laboratorios Zeyco, S.A. de C.V manufacture?
3 registered sites are on record, in United Arab Emirates and Mexico (Zapopan and Mexico among others). Every site is listed on this page with the register it came from.
Which regulators recognise Laboratorios Zeyco, S.A. de C.V's GMP?
Current GMP certificates are on record from MFDS (Korea), COFEPRIS (MX) and US FDA. 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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Open risk flags

  • The most recent inspection outcome was NAI, on 10 November 2023.

Comparable suppliers

Abbott Laboratories De México, S. A. De C. V also in Mexico Armstrong Laboratorios De México, S.A. De C.V also in Mexico Bayer De Mexico, S.A. De C.V also in Mexico Fermic, s.a. de c.v also in Mexico Grimann, S.A. de C.V also in Mexico

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