Suppliers / Pt. Actavis Indonesia

Pt. Actavis Indonesia

Indonesia 257 employees Updated 9 July 2026

Pt. Actavis Indonesia is a finished-dose manufacturer based in Indonesia. It appears in 17 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with DAV (Vietnam), NPRA (MY) and RCETH (BY). Its GMP standing is certified by BPOM (ID), EAEU_EEC and EMA. Customs aggregates show $552K of exports covering 23 molecules to 6 destinations in 2025.

0
active US DMFs
0
valid CEPs
1
registered plants
17
filings across 3 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
Jakarta, Indonesia Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 14 None
NPRA (MY) 2 None
RCETH (BY) 1 None
BPOM (ID) None 16
EAEU_EEC None 1
EMA None 1

Scale

Year Revenue Exports Destinations
2025 Not reported $552K 6
2024 Not reported $2.0M 6

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 We do not publish the identity of any buyer.

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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
Customs aggregates
Export values, molecule and destination counts