LABORATORIO TEUTO BRASILEIRO S/A
Brasilianischer Hersteller von Arzneimitteln für den menschlichen Gebrauch
LABORATORIO TEUTO BRASILEIRO S/A ist ein brasilianischer Hersteller, der sich auf die Herstellung von alopátischen Arzneimitteln für den menschlichen Gebrauch spezialisiert hat und seinen Sitz in ANAPOLIS hat. Gelistet im offiziellen Receita Federal CNPJ-Register Brasiliens; bedient den heimischen Markt und ist offen für B2B-Großhandelsvertriebspartnerschaften.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- ANAPOLIS, Brazil
- Website
- https://teuto.com.br
- Categories
- Pharmazeutische Produktion
- Markets
- Brasilien
Listed in a source registry
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
- domain-registered (green), checked 2026-08-02 Domain registry record
- energy-market-consumer (green), effective since 2026-08-01 CCEE (Câmara de Comercialização de Energia Elétrica)
- registry-active-global (green), checked 2026-08-13 CCEE (Câmara de Comercialização de Energia Elétrica)
- cnpj-active (green), checked 2026-07-20 Receita Federal (CNPJ)
- registry-activity (green), checked 2026-07-20 Receita Federal (CNPJ)
- directors-on-file (green), checked 2026-07-20 Receita Federal (CNPJ)
- registry-id-verified (green), checked 2026-08-13 CCEE (Câmara de Comercialização de Energia Elétrica)
- development-project-financed (green), checked 2026-08-28 BNDES, Banco Nacional de Desenvolvimento Econômico e Social, Portal de Dados Abertos (operações não automáticas)
- tax-debt-published (red), checked 2026-09-22 Brazilian National Treasury Attorney's Office (PGFN), active federal debt register
Import rules for these goods
- Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)