Suppliers / S Kant Healthcare

S Kant Healthcare

India 270 employees 2 duplicate records merged Updated 9 July 2026

S Kant Healthcare is a finished-dose manufacturer based in India. It appears in 134 regulatory filings across 8 regulators, without an active US DMF or CEP on file. Its filings concentrate with TMDA (TZ), NAFDAC (NG) and EFDA (ET). Its GMP standing is certified by NAFDAC (NG), FDA (GH) and TMDA (TZ), among 4 authorities. Customs aggregates show $46.5M of exports covering 1,092 molecules to 66 destinations in 2025.

0
active US DMFs
0
valid CEPs
2
registered plants
134
filings across 8 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
Vapi, India Not on file
Gujarat State, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
TMDA (TZ) 55 1
NAFDAC (NG) 26 2
EFDA (ET) 25 None
DIGEMAPS (DO) 18 None
UZPHARM (UZ) 4 None
MINSA (CR) 3 None
FDA (GH) None 1
EMA None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $13.0M 28
2025 Not reported $46.5M 66
2024 Not reported $44.7M 54
2023 Not reported $39.8M 51

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 We do not publish the identity of any buyer.

Questions about S Kant Healthcare

Does S Kant Healthcare hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for S Kant Healthcare. It does have 134 filings with 8 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does S Kant Healthcare manufacture?
2 registered sites are on record, in India and Nigeria (Vapi and Gujarat State). Every site is listed on this page with the register it came from.
Which regulators recognise S Kant Healthcare's GMP?
Current GMP certificates are on record from NAFDAC (NG), FDA (GH), TMDA (TZ) and EMA. 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