Suppliers / VARIA SEKATA PHARMACEUTICAL LABORATORIES - Indonesia

VARIA SEKATA PHARMACEUTICAL LABORATORIES - Indonesia

Indonesia Updated 9 July 2026

VARIA SEKATA PHARMACEUTICAL LABORATORIES - Indonesia is a finished-dose manufacturer based in Indonesia. It appears in 1 regulatory filing across 1 regulator, without an active US DMF or CEP on file.

0
active US DMFs
0
valid CEPs
1
registered plants
1
filings across 1 regulators

Registered plants

Site FDA FEI
-, Indonesia Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
BPOM (ID) 1 None

Questions about VARIA SEKATA PHARMACEUTICAL LABORATORIES - Indonesia

Does VARIA SEKATA PHARMACEUTICAL LABORATORIES - Indonesia hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for VARIA SEKATA PHARMACEUTICAL LABORATORIES - Indonesia. It does have 1 filing with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does VARIA SEKATA PHARMACEUTICAL LABORATORIES - Indonesia manufacture?
1 registered site is on record, in Indonesia (-). Every site is listed on this page with the register it came from.
Where does VARIA SEKATA PHARMACEUTICAL LABORATORIES - Indonesia file?
Filings are on record with BPOM (ID), 1 in total.

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.

Checking VARIA SEKATA PHARMACEUTICAL LABORATORIES - Indonesia?

Ask Fred what the record holds on VARIA SEKATA PHARMACEUTICAL LABORATORIES - Indonesia, including filings and inspection history.

Chat with Fred, your AI analyst
Opens WhatsApp. Free to start.

Comparable suppliers

Dankos Farma also in Indonesia Dexa Medica also in Indonesia Ferron Par Pharmaceuticals also in Indonesia Fonko International Pharmaceuticals also in Indonesia Medikon Prima Laboratories 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