Suppliers / Interphil Laboratories

Interphil Laboratories

Philippines 179 employees Updated 9 July 2026

Interphil Laboratories is a finished-dose manufacturer based in Philippines. It appears in 4 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with NPRA (MY) and EEC_EAEU.

0
active US DMFs
0
valid CEPs
0
registered plants
4
filings across 2 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
NPRA (MY) 2 None
EEC_EAEU 2 None

Limited public record

Beyond the filing counts above, the public registers hold no plant, inspection or portfolio detail for this company as at 9 July 2026. We report that as a gap rather than inferring an answer.

Questions about Interphil Laboratories

Does Interphil Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Interphil Laboratories. It does have 4 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Interphil Laboratories file?
Filings are on record with NPRA (MY) and EEC (Eurasian Economic Union), 4 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.

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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability