Suppliers / Kesar Pharma

Kesar Pharma

India 2 duplicate records merged Updated 9 July 2026

Kesar Pharma is a finished-dose manufacturer based in India. It appears in 79 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with NAFDAC (NG), FDA (GH) and DIGEMAPS (DO). Its GMP standing is certified by CDSCO (India) and NAFDAC (NG). Customs aggregates show $137K of exports covering 5 molecules to 3 destinations in 2025.

0
active US DMFs
0
valid CEPs
2
registered plants
79
filings across 5 regulators

Registered plants

Site FDA FEI
l kalolbileshwarpur a 382 729gandhinagar, India Not on file
GANDHINAGAR, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
NAFDAC (NG) 50 1
FDA (GH) 19 None
DIGEMAPS (DO) 6 None
UZPHARM (UZ) 3 None
ARCSA (EC) 1 None
CDSCO (India) None 2

Scale

Year Revenue Exports Destinations
2025 Not reported $137K 3
2024 Not reported $395K 4
2023 Not reported $1.0M 3
2022 Not reported $2.2M 6

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 We do not publish the identity of any buyer.

Questions about Kesar Pharma

Does Kesar Pharma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Kesar Pharma. It does have 79 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Kesar Pharma manufacture?
2 registered sites are on record, in India and Nigeria (L Kalolbileshwarpur A 382 729gandhinagar and Gandhinagar). Every site is listed on this page with the register it came from.
Which regulators recognise Kesar Pharma's GMP?
Current GMP certificates are on record from CDSCO (India) and NAFDAC (NG). 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