Suppliers / Oxford Laboratories

Oxford Laboratories

India 3 employees 2 duplicate records merged Updated 9 July 2026

Oxford Laboratories is a finished-dose manufacturer based in India. It appears in 51 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with UZPHARM (UZ), EFDA (ET) and EEC_EAEU. Its GMP standing is certified by CDSCO (India), EAEU_EEC and UZPHARM (UZ). Customs aggregates show $6.8M of exports covering 493 molecules to 12 destinations in 2025.

0
active US DMFs
0
valid CEPs
4
registered plants
51
filings across 3 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
at indradtal kadimehsana 382 715, India Not on file
mehsan a, India Not on file
valsad 396 125, India Not on file
vadoda ra, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
UZPHARM (UZ) 44 1
EFDA (ET) 6 None
EEC_EAEU 1 None
CDSCO (India) None 5
EAEU_EEC None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $1.5M 9
2025 Not reported $6.8M 12
2024 Not reported $7.4M 11
2023 Not reported $5.5M 13

Export figures are customs aggregates. We do not publish the identity of any buyer.

Questions about Oxford Laboratories

Does Oxford Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Oxford Laboratories. It does have 51 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Oxford Laboratories manufacture?
4 registered sites are on record, in India (At Indradtal Kadimehsana 382 715, Mehsan A and Valsad 396 125 among others). Every site is listed on this page with the register it came from.
Which regulators recognise Oxford Laboratories's GMP?
Current GMP certificates are on record from CDSCO (India), EEC (Eurasian Economic Union) and UZPHARM (UZ). 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
Customs aggregates
Export values, molecule and destination counts