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 We do not publish the identity of any buyer.

Questions about Pt. Actavis Indonesia

Does Pt. Actavis Indonesia hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Pt. Actavis Indonesia. It does have 17 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Pt. Actavis Indonesia manufacture?
1 registered site is on record, in Indonesia (Jakarta). Every site is listed on this page with the register it came from.
Which regulators recognise Pt. Actavis Indonesia's GMP?
Current GMP certificates are on record from BPOM (ID), EEC (Eurasian Economic Union) and EMA. 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
Customs aggregates
Export values, molecule and destination counts