Suppliers / Takeda Pharma Ltda

Takeda Pharma Ltda

Brazil Updated 9 July 2026

Takeda Pharma Ltda is a finished-dose manufacturer based in Brazil. It appears in 1,146 regulatory filings across 19 regulators, without an active US DMF or CEP on file. Its filings concentrate with ANVISA (Brazil), SWISSMEDIC (CH) and AIFA (IT). Its GMP standing is certified by ANVISA (Brazil) and INVIMA (CO).

0
active US DMFs
0
valid CEPs
4
registered plants
1,146
filings across 19 regulators

Registered plants

Site FDA FEI
JAGUARIUNA, Brazil Not on file
JAGUARIÚNA, Brazil Not on file
Opfikon, Switzerland Not on file
Jaguariuna, Colombia Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ANVISA (Brazil) 305 4
SWISSMEDIC (CH) 175 None
AIFA (IT) 162 None
FAMHP (BE) 143 None
AEMPS (ES) 140 None
DKMA (DK) 80 None
INVIMA (CO) None 1

Questions about Takeda Pharma Ltda

Does Takeda Pharma Ltda hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Takeda Pharma Ltda. It does have 1,146 filings with 19 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Takeda Pharma Ltda manufacture?
4 registered sites are on record, in Brazil, Switzerland and Colombia (Jaguariuna, Jaguariúna and Opfikon among others). Every site is listed on this page with the register it came from.
Which regulators recognise Takeda Pharma Ltda's GMP?
Current GMP certificates are on record from ANVISA (Brazil) and INVIMA (CO). 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