Suppliers / Taisho Pharmaceutical

Taisho Pharmaceutical

Japan Updated 9 July 2026

Taisho Pharmaceutical is a finished-dose manufacturer based in Japan. It appears in 108 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with BPOM (ID), DH (HK) and NPRA (MY). Its GMP standing is certified by HSA (SG).

0
active US DMFs
0
valid CEPs
2
registered plants
108
filings across 3 regulators

Registered plants

Site FDA FEI
KOTA DEPOK, Indonesia Not on file
-, Indonesia Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
BPOM (ID) 53 None
DH (HK) 53 None
NPRA (MY) 2 None
HSA (SG) None 2

Questions about Taisho Pharmaceutical

Does Taisho Pharmaceutical hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Taisho Pharmaceutical. It does have 108 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Taisho Pharmaceutical manufacture?
2 registered sites are on record, in Indonesia (Kota Depok and -). Every site is listed on this page with the register it came from.
Which regulators recognise Taisho Pharmaceutical's GMP?
Current GMP certificates are on record from HSA (SG). 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