Suppliers / Dankos Farma

Dankos Farma

Indonesia Updated 9 July 2026

Dankos Farma is a finished-dose manufacturer based in Indonesia. It appears in 123 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with BPOM (ID), NPRA (MY) and NAFDAC (NG). Its GMP standing is certified by BPOM (ID) and NAFDAC (NG). Customs aggregates show $29K of exports covering 2 molecules to 2 destinations in 2025.

0
active US DMFs
0
valid CEPs
2
registered plants
123
filings across 3 regulators

Registered plants

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

Filings and GMP by regulator

Regulator Filings GMP certificates
BPOM (ID) 117 32
NPRA (MY) 5 None
NAFDAC (NG) 1 1

Scale

Year Revenue Exports Destinations
2025 Not reported $29K 2
2024 Not reported $340K 4

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 We do not publish the identity of any buyer.

Questions about Dankos Farma

Does Dankos Farma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Dankos Farma. It does have 123 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Dankos Farma manufacture?
2 registered sites are on record, in Indonesia (- and Kodya Jakarta Timur). Every site is listed on this page with the register it came from.
Which regulators recognise Dankos Farma'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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Comparable suppliers

Dexa Medica also in Indonesia Ferron Par Pharmaceuticals also in Indonesia Fonko International Pharmaceuticals also in Indonesia Medikon Prima Laboratories also in Indonesia Meiji Indonesian Pharmaceutical Industries 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