Suppliers / Xl Laboratories

Xl Laboratories

India 235 employees 2 duplicate records merged Updated 9 July 2026

Xl Laboratories is a finished-dose manufacturer based in India. It appears in 181 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with DAV (Vietnam), EFDA (ET) and JFDA (JO). Its GMP standing is certified by EMA, FDA (GH) and ANVISA (Brazil). Customs aggregates show $10.4M of exports covering 555 molecules to 29 destinations in 2025.

0
active US DMFs
0
valid CEPs
3
registered plants
181
filings across 6 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
ALWAR, India Not on file
Bhiwadi, India Not on file
Neemrana, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 169 None
EFDA (ET) 4 None
JFDA (JO) 3 None
TMDA (TZ) 2 None
MINSA (CR) 2 None
ARCSA (EC) 1 None
EMA None 5
FDA (GH) None 2
ANVISA (Brazil) None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $1.5M 17
2025 Not reported $10.4M 29
2024 Not reported $10.7M 25
2023 Not reported $8.3M 24

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 We do not publish the identity of any buyer.

Questions about Xl Laboratories

Does Xl Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Xl Laboratories. It does have 181 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Xl Laboratories manufacture?
3 registered sites are on record, in India (Alwar, Bhiwadi and Neemrana). Every site is listed on this page with the register it came from.
Which regulators recognise Xl Laboratories's GMP?
Current GMP certificates are on record from EMA, FDA (GH) and ANVISA (Brazil). 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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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
EudraGMDP and national regulators
GMP certificates
Customs aggregates
Export values, molecule and destination counts