Suppliers / Pt Tunggal Idaman Abdi

Pt Tunggal Idaman Abdi

Indonesia 423 employees Updated 9 July 2026

Pt Tunggal Idaman Abdi is a finished-dose manufacturer based in Indonesia. It appears in 118 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with BPOM (ID), EFDA (ET) and DIGEMAPS (DO). Its GMP standing is certified by BPOM (ID) and NAFDAC (NG). Customs aggregates show $5.2M of exports covering 20 molecules to 7 destinations in 2025.

0
active US DMFs
0
valid CEPs
3
registered plants
118
filings across 4 regulators

Registered plants

Site FDA FEI
KODYA JAKARTA TIMUR, Indonesia Not on file
KOTA BOGOR, Indonesia Not on file
-, Indonesia Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
BPOM (ID) 115 22
EFDA (ET) 1 None
DIGEMAPS (DO) 1 None
NAFDAC (NG) 1 1

Scale

Year Revenue Exports Destinations
2025 Not reported $5.2M 7
2024 Not reported $6.4M 5

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 We do not publish the identity of any buyer.

Questions about Pt Tunggal Idaman Abdi

Does Pt Tunggal Idaman Abdi hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Pt Tunggal Idaman Abdi. It does have 118 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Pt Tunggal Idaman Abdi manufacture?
3 registered sites are on record, in Indonesia (Kodya Jakarta Timur, Kota Bogor and -). Every site is listed on this page with the register it came from.
Which regulators recognise Pt Tunggal Idaman Abdi's GMP?
Current GMP certificates are on record from BPOM (ID) and NAFDAC (NG). 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