Suppliers / Laboratorio Industrial Farmaceutico De Alagoas

Laboratorio Industrial Farmaceutico De Alagoas

Brazil Updated 9 July 2026

Laboratorio Industrial Farmaceutico De Alagoas is a finished-dose manufacturer based in Brazil. It appears in 67 regulatory filings across 1 regulator, without an active US DMF or CEP on file.

0
active US DMFs
0
valid CEPs
1
registered plants
67
filings across 1 regulators

Registered plants

Site FDA FEI
MACEIO, Brazil Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ANVISA (Brazil) 67 None

Questions about Laboratorio Industrial Farmaceutico De Alagoas

Does Laboratorio Industrial Farmaceutico De Alagoas hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorio Industrial Farmaceutico De Alagoas. It does have 67 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratorio Industrial Farmaceutico De Alagoas manufacture?
1 registered site is on record, in Brazil (Maceio). Every site is listed on this page with the register it came from.
Where does Laboratorio Industrial Farmaceutico De Alagoas file?
Filings are on record with ANVISA (Brazil), 67 in total.

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.

Checking Laboratorio Industrial Farmaceutico De Alagoas?

Ask Fred what the record holds on Laboratorio Industrial Farmaceutico De Alagoas, including filings and inspection history.

Chat with Fred, your AI analyst
Opens WhatsApp. Free to start.

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