Suppliers / KLM Laboratories

KLM Laboratories

India 674 employees 3 duplicate records merged Updated 9 July 2026

KLM Laboratories is a finished-dose manufacturer based in India. It appears in 25 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with EFDA (ET), TMDA (TZ) and ARCSA (EC). Its GMP standing is certified by CDSCO (India) and TMDA (TZ). Customs aggregates show $1.3M of exports covering 276 molecules to 9 destinations in 2025.

0
active US DMFs
0
valid CEPs
4
registered plants 2 with an FDA FEI number
25
filings across 6 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
2 of 2 confirmed
Sources: FDA Establishment Registration, read 4 May 2026.

Registered plants

Site FDA FEI
Vadodara, India 3017001542
Vadodara, India 3032592163
Plot No., India Not on file
near bamangamtal karjanvadodara 391 243, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EFDA (ET) 11 None
TMDA (TZ) 6 1
ARCSA (EC) 3 None
ZAMRA (ZM) 3 None
US FDA 1 None
NAFDAC (NG) 1 None
CDSCO (India) None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $35K 2
2025 Not reported $1.3M 9
2024 Not reported $904K 12
2023 Not reported $727K 8

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 We do not publish the identity of any buyer.

Questions about KLM Laboratories

Does KLM Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for KLM Laboratories. It does have 25 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is KLM Laboratories FDA-registered?
2 sites operated by KLM Laboratories carry an FDA establishment identifier (FEI), which means they are registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
Where does KLM Laboratories manufacture?
4 registered sites are on record, in India (Vadodara, Plot No. and Near Bamangamtal Karjanvadodara 391 243 among others). Every site is listed on this page with the register it came from.
Which regulators recognise KLM Laboratories's GMP?
Current GMP certificates are on record from CDSCO (India) and TMDA (TZ). 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