Suppliers / Menarini Indria Laboratories

Menarini Indria Laboratories

Indonesia Updated 9 July 2026

Menarini Indria Laboratories is a finished-dose manufacturer based in Indonesia. It appears in 95 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with BPOM (ID) and NPRA (MY). Its GMP standing is certified by BPOM (ID). Customs aggregates show $1.2M of exports covering 36 molecules to 3 destinations in 2025.

0
active US DMFs
0
valid CEPs
2
registered plants
95
filings across 2 regulators

Registered plants

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

Filings and GMP by regulator

Regulator Filings GMP certificates
BPOM (ID) 94 6
NPRA (MY) 1 None

Scale

Year Revenue Exports Destinations
2025 Not reported $1.2M 3
2024 Not reported $2.2M 4

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 We do not publish the identity of any buyer.

Questions about Menarini Indria Laboratories

Does Menarini Indria Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Menarini Indria Laboratories. It does have 95 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Menarini Indria Laboratories manufacture?
2 registered sites are on record, in Indonesia (- and Kab. Bekasi). Every site is listed on this page with the register it came from.
Which regulators recognise Menarini Indria Laboratories's GMP?
Current GMP certificates are on record from BPOM (ID). 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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Comparable suppliers

Dankos Farma also in Indonesia Dexa Medica also in Indonesia Ferron Par Pharmaceuticals also in Indonesia Fonko International Pharmaceuticals also in Indonesia Medikon Prima Laboratories also in Indonesia

Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

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