Suppliers / Murli Krishna Pharma

Murli Krishna Pharma

India 183 employees Updated 9 July 2026

Murli Krishna Pharma is an API manufacturer based in India. It holds 9 active US drug master files across a filed portfolio of 8 molecules. Its GMP standing is certified by EMA. Customs aggregates show $19.0M of exports covering 349 molecules to 41 destinations in 2025.

9
active US DMFs
0
valid CEPs
1
registered plants
1
filings across 1 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
Ranjangaon Taluka Shirur, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 1 None
EMA None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $4.7M 17
2025 Not reported $19.0M 41
2024 Not reported $13.4M 32
2023 Not reported $14.9M 33

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 We do not publish the identity of any buyer.

Questions about Murli Krishna Pharma

Does Murli Krishna Pharma hold a US DMF or a CEP?
Murli Krishna Pharma holds 9 active US drug master files. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Where does Murli Krishna Pharma manufacture?
1 registered site is on record, in India (Ranjangaon Taluka Shirur). Every site is listed on this page with the register it came from.
What does Murli Krishna Pharma make?
8 molecules are on record against Murli Krishna Pharma, including Orlistat, Clarithromycin, Duloxetine and Esomeprazole. Each links through to that molecule's full manufacturer list.
Which regulators recognise Murli Krishna Pharma's GMP?
Current GMP certificates are on record from 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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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