Suppliers / Ashford Pharmaceutical Laboratories

Ashford Pharmaceutical Laboratories

Philippines Updated 9 July 2026

Ashford Pharmaceutical Laboratories is a finished-dose manufacturer based in Philippines. It appears in 26 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with FDA (GH) and NAFDAC (NG). Its GMP standing is certified by NAFDAC (NG).

0
active US DMFs
0
valid CEPs
0
registered plants
26
filings across 2 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
FDA (GH) 14 None
NAFDAC (NG) 12 1

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 Ashford Pharmaceutical Laboratories

Does Ashford Pharmaceutical Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Ashford Pharmaceutical Laboratories. It does have 26 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Which regulators recognise Ashford Pharmaceutical Laboratories'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