Suppliers / Kusum Healthcare

Kusum Healthcare

India Updated 9 July 2026

Kusum Healthcare is a finished-dose manufacturer based in India. It appears in 190 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with UZPHARM (UZ), DAV (Vietnam) and TMDA (TZ). Its GMP standing is certified by NCELS (KZ), EMA and UZPHARM (UZ). Customs aggregates show $64.5M of exports covering 2,933 molecules to 22 destinations in 2025.

0
active US DMFs
0
valid CEPs
2
registered plants
190
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
Dhar, India Not on file
Bhiwadi, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
UZPHARM (UZ) 104 3
DAV (Vietnam) 33 None
TMDA (TZ) 26 None
EFDA (ET) 20 None
NCELS (KZ) 5 4
CDSCO (India) 2 None
EMA None 3

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $9.0M 13
2025 Not reported $64.5M 22
2024 Not reported $56.5M 19
2023 Not reported $53.2M 16

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 We do not publish the identity of any buyer.

Questions about Kusum Healthcare

Does Kusum Healthcare hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Kusum Healthcare. It does have 190 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Kusum Healthcare manufacture?
2 registered sites are on record, in India (Dhar and Bhiwadi). Every site is listed on this page with the register it came from.
Which regulators recognise Kusum Healthcare's GMP?
Current GMP certificates are on record from NCELS (KZ), EMA 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