Suppliers / Laboratorio Teuto Brasileiro S/A

Laboratorio Teuto Brasileiro S/A

Brazil 45 employees Updated 9 July 2026

Laboratorio Teuto Brasileiro S/A is a finished-dose manufacturer based in Brazil. It appears in 1,483 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with ANVISA (Brazil) and ARCSA (EC). Its GMP standing is certified by ANVISA (Brazil).

0
active US DMFs
0
valid CEPs
1
registered plants
1,483
filings across 2 regulators

Registered plants

Site FDA FEI
ANAPOLIS, Brazil Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ANVISA (Brazil) 1,479 4
ARCSA (EC) 4 None

Questions about Laboratorio Teuto Brasileiro S/A

Does Laboratorio Teuto Brasileiro S/A hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorio Teuto Brasileiro S/A. It does have 1,483 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratorio Teuto Brasileiro S/A manufacture?
1 registered site is on record, in Brazil (Anapolis). Every site is listed on this page with the register it came from.
Which regulators recognise Laboratorio Teuto Brasileiro S/A's GMP?
Current GMP certificates are on record from 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.

Comparing suppliers?

Choose your molecules and target markets. Laboratorio Teuto Brasileiro S/A comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Comparable suppliers

Abbott Laboratorios Do Brasil Ltda also in Brazil Aché Laboratorios Farmacéuticos S. A also in Brazil Alcon Laboratórios Do Brasil Ltda also in Brazil Allergan Produtos Farmaceuticos Ltda also in Brazil Baxter Hospitalar Ltda also in Brazil

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