Suppliers / Sandoz Do Brasil Industria Farmaceutica Ltda

Sandoz Do Brasil Industria Farmaceutica Ltda

Brazil Updated 9 July 2026

The public registers hold a second record for Sandoz Do Brasil Industria Farmaceutica Ltda. The fuller profile, with 40 active US DMFs and 20 valid CEPs, is at Sandoz. Figures on this page cover only this record.

Sandoz Do Brasil Industria Farmaceutica Ltda is a finished-dose manufacturer based in Brazil. It appears in 1,799 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with ANVISA (Brazil), AEMPS (ES) and EMA. Its GMP standing is certified by EMA and ANVISA (Brazil).

0
active US DMFs
0
valid CEPs
1
registered plants
1,799
filings across 5 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
CAMBE, Brazil Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ANVISA (Brazil) 969 1
AEMPS (ES) 743 None
EMA 77 1
ARCSA (EC) 6 None
MINSA (CR) 4 None

Questions about Sandoz Do Brasil Industria Farmaceutica Ltda

Does Sandoz Do Brasil Industria Farmaceutica Ltda hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Sandoz Do Brasil Industria Farmaceutica Ltda. It does have 1,799 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Sandoz Do Brasil Industria Farmaceutica Ltda manufacture?
1 registered site is on record, in Brazil (Cambe). Every site is listed on this page with the register it came from.
Which regulators recognise Sandoz Do Brasil Industria Farmaceutica Ltda's GMP?
Current GMP certificates are on record from EMA 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