Suppliers / Pt Kimia Farma Persero Tbk

Pt Kimia Farma Persero Tbk

Indonesia 56 employees Updated 9 July 2026

Pt Kimia Farma Persero Tbk is an API and finished-dose manufacturer based in Indonesia. It appears in 10 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with CDSCO (India) and NAFDAC (NG). Its GMP standing is certified by NAFDAC (NG).

0
active US DMFs
0
valid CEPs
0
registered plants
10
filings across 2 regulators

What they file, and where

Molecule Regulators Docs
Prucalopride SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Bempedoic Acid finished dose Obeticholic Acid finished dose Prucalopride API

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) 9 None
NAFDAC (NG) 1 1

Questions about Pt Kimia Farma Persero Tbk

Does Pt Kimia Farma Persero Tbk hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Pt Kimia Farma Persero Tbk. It does have 10 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
What does Pt Kimia Farma Persero Tbk make?
1 molecule is on record against Pt Kimia Farma Persero Tbk, including Prucalopride. Each links through to that molecule's full manufacturer list.
Which regulators recognise Pt Kimia Farma Persero Tbk's GMP?
Current GMP certificates are on record from 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