Suppliers / Kilitch Drugs (India)

Kilitch Drugs (India)

India 305 employees 2 duplicate records merged Updated 9 July 2026

Kilitch Drugs (India) is a finished-dose manufacturer based in India. It appears in 71 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with EFDA (ET), NAFDAC (NG) and EEC_EAEU. Its GMP standing is certified by NAFDAC (NG), CDSCO (India) and FDA (GH). Customs aggregates show $15.7M of exports covering 575 molecules to 26 destinations in 2025.

0
active US DMFs
0
valid CEPs
3
registered plants
71
filings across 5 regulators

Registered plants

Site FDA FEI
Survey No, India Not on file
hodiyar colonylakhabavad 361 006jamnagar, India Not on file
Navi Mumbai, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EFDA (ET) 57 None
NAFDAC (NG) 10 2
EEC_EAEU 2 None
MCAZ (ZW) 1 None
DIGEMAPS (DO) 1 None
CDSCO (India) None 2
FDA (GH) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $4.1M 16
2025 Not reported $15.7M 26
2024 Not reported $15.1M 30
2023 Not reported $14.7M 27

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 We do not publish the identity of any buyer.

Questions about Kilitch Drugs (India)

Does Kilitch Drugs (India) hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Kilitch Drugs (India). It does have 71 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Kilitch Drugs (India) manufacture?
3 registered sites are on record, in India and Nigeria (Survey No, Hodiyar Colonylakhabavad 361 006jamnagar and Navi Mumbai). Every site is listed on this page with the register it came from.
Which regulators recognise Kilitch Drugs (India)'s GMP?
Current GMP certificates are on record from NAFDAC (NG), CDSCO (India) and FDA (GH). 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