Suppliers / Abbott Laboratories De México, S. A. De C. V

Abbott Laboratories De México, S. A. De C. V

Mexico Updated 9 July 2026

Abbott Laboratories De México, S. A. De C. V is a finished-dose manufacturer based in Mexico. It appears in 91 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO), MINSA (CR) and COFEPRIS (MX). Its GMP standing is certified by COFEPRIS (MX) and ANVISA (Brazil). Customs aggregates show $225K of exports covering 2 molecules to 2 destinations in 2024.

0
active US DMFs
0
valid CEPs
3
registered plants
91
filings across 5 regulators

Registered plants

Site FDA FEI
MEXICO CITY (DISTRITO FEDERAL), Mexico Not on file
Coyoacán, Mexico Not on file
Cuautitlán Izcalli, Mexico Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 52 None
MINSA (CR) 35 None
COFEPRIS (MX) 2 2
SFDA (Saudi Arabia) 1 None
INVIMA (CO) 1 None
ANVISA (Brazil) None 2

Scale

Year Revenue Exports Destinations
2024 Not reported $225K 2
2023 Not reported $28.9M 21
2022 Not reported $25.1M 18

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 We do not publish the identity of any buyer.

Questions about Abbott Laboratories De México, S. A. De C. V

Does Abbott Laboratories De México, 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 Abbott Laboratories De México, S. A. De C. V. It does have 91 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Abbott Laboratories De México, S. A. De C. V manufacture?
3 registered sites are on record, in Mexico (Mexico City (distrito Federal), Coyoacán and Cuautitlán Izcalli). Every site is listed on this page with the register it came from.
Which regulators recognise Abbott Laboratories De México, S. A. De C. V's GMP?
Current GMP certificates are on record from COFEPRIS (MX) and ANVISA (Brazil). 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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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