Suppliers / Neon Laboratories

Neon Laboratories

India 3 duplicate records merged Updated 9 July 2026

Neon Laboratories is a finished-dose manufacturer based in India. It appears in 63 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with EFDA (ET), JFDA (JO) and MINSA (CR). Customs aggregates show $8.5M of exports covering 788 molecules to 39 destinations in 2025.

0
active US DMFs
0
valid CEPs
0
registered plants
63
filings across 6 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
EFDA (ET) 31 None
JFDA (JO) 21 None
MINSA (CR) 5 None
ZAMRA (ZM) 3 None
CDSCO (India) 2 None
ARCSA (EC) 1 None

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $873K 16
2025 Not reported $8.5M 39
2024 Not reported $7.5M 35
2023 Not reported $5.8M 38

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 We do not publish the identity of any buyer.

Limited public record

Beyond the filing counts above, the public registers hold no plant, inspection or portfolio detail for this company as at 9 July 2026. We report that as a gap rather than inferring an answer.

Questions about Neon Laboratories

Does Neon Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Neon Laboratories. It does have 63 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Neon Laboratories file?
Filings are on record with EFDA (ET), JFDA (JO), MINSA (CR), ZAMRA (ZM) and 2 other regulators, 63 in total.

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
Customs aggregates
Export values, molecule and destination counts