Suppliers / Dfl Industria E Comercio S/A

Dfl Industria E Comercio S/A

Brazil Updated 9 July 2026

Dfl Industria E Comercio S/A is a finished-dose manufacturer based in Brazil. It appears in 77 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with ANVISA (Brazil), RAMA (GE) and ARCSA (EC). Its GMP standing is certified by ANVISA (Brazil) and NAFDAC (NG).

0
active US DMFs
0
valid CEPs
1
registered plants
77
filings across 6 regulators

Registered plants

Site FDA FEI
RIO DE JANEIRO, Brazil Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ANVISA (Brazil) 41 2
RAMA (GE) 20 None
ARCSA (EC) 8 None
MINSA (CR) 5 None
DIGEMAPS (DO) 2 None
NAFDAC (NG) 1 1

Questions about Dfl Industria E Comercio S/A

Does Dfl Industria E Comercio S/A hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Dfl Industria E Comercio S/A. It does have 77 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Dfl Industria E Comercio S/A manufacture?
1 registered site is on record, in Brazil (RIO DE Janeiro). Every site is listed on this page with the register it came from.
Which regulators recognise Dfl Industria E Comercio S/A's GMP?
Current GMP certificates are on record from ANVISA (Brazil) and NAFDAC (NG). 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