Suppliers / Meiji Indonesian Pharmaceutical Industries

Meiji Indonesian Pharmaceutical Industries

Indonesia Updated 9 July 2026

Meiji Indonesian Pharmaceutical Industries is a finished-dose manufacturer based in Indonesia. It appears in 76 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Customs aggregates show $3.9M of exports covering 38 molecules to 1 destination in 2025.

0
active US DMFs
0
valid CEPs
2
registered plants
76
filings across 1 regulators

Registered plants

Site FDA FEI
KAB. PASURUAN, Indonesia Not on file
-, Indonesia Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
BPOM (ID) 76 None

Scale

Year Revenue Exports Destinations
2025 Not reported $3.9M 1

Export figures are customs aggregates. We do not publish the identity of any buyer.

Questions about Meiji Indonesian Pharmaceutical Industries

Does Meiji Indonesian Pharmaceutical Industries hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Meiji Indonesian Pharmaceutical Industries. It does have 76 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Meiji Indonesian Pharmaceutical Industries manufacture?
2 registered sites are on record, in Indonesia (Kab. Pasuruan and -). Every site is listed on this page with the register it came from.
Where does Meiji Indonesian Pharmaceutical Industries file?
Filings are on record with BPOM (ID), 76 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.

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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
Customs aggregates
Export values, molecule and destination counts