Suppliers / Luna Chemical Industries

Luna Chemical Industries

India 2 duplicate records merged Updated 9 July 2026

Luna Chemical Industries is an API manufacturer based in India. It holds one active US drug master file and one valid CEP. Its GMP standing is certified by CDSCO (India). Customs aggregates show $3.0M of exports covering 55 molecules to 11 destinations in 2025.

1
active US DMFs
1
valid CEPs
2
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Bharuch, India Not on file
Bharuch, India Not on file

What they file, and where

Molecule Regulators Docs
Ibuprofen EDQM, US FDA 2

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $168K 3
2025 Not reported $3.0M 11
2024 Not reported $1.5M 11
2023 Not reported $1.0M 6

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 We do not publish the identity of any buyer.

Questions about Luna Chemical Industries

Does Luna Chemical Industries hold a US DMF or a CEP?
Luna Chemical Industries holds 1 active US drug master file and 1 valid CEP. 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 Luna Chemical Industries manufacture?
2 registered sites are on record, in India (Bharuch among others). Every site is listed on this page with the register it came from.
What does Luna Chemical Industries make?
1 molecule is on record against Luna Chemical Industries, including Ibuprofen. Each links through to that molecule's full manufacturer list.
Which regulators recognise Luna Chemical Industries's GMP?
Current GMP certificates are on record from CDSCO (India). 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