Suppliers / PT Nulab Pharmaceutical Indonesia

PT Nulab Pharmaceutical Indonesia

Indonesia 184 employees Updated 9 July 2026

PT Nulab Pharmaceutical Indonesia is a finished-dose manufacturer based in Indonesia. It appears in 165 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with BPOM (ID), EEC_EAEU and INVIMA (CO). Its GMP standing is certified by BPOM (ID).

0
active US DMFs
0
valid CEPs
2
registered plants
165
filings across 3 regulators

Registered plants

Site FDA FEI
-, Indonesia Not on file
KOTA TANGERANG, Indonesia Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
BPOM (ID) 161 4
EEC_EAEU 3 None
INVIMA (CO) 1 None

Questions about PT Nulab Pharmaceutical Indonesia

Does PT Nulab Pharmaceutical Indonesia hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for PT Nulab Pharmaceutical Indonesia. It does have 165 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does PT Nulab Pharmaceutical Indonesia manufacture?
2 registered sites are on record, in Indonesia (- and Kota Tangerang). Every site is listed on this page with the register it came from.
Which regulators recognise PT Nulab Pharmaceutical Indonesia's GMP?
Current GMP certificates are on record from BPOM (ID). 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