Suppliers / Oneiro Chemicals

Oneiro Chemicals

India Updated 9 July 2026

Oneiro Chemicals is a finished-dose manufacturer based in India. It appears in 6 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with CDSCO (India) and MINSA (CR). Its GMP standing is certified by CDSCO (India). Customs aggregates show $3.4M of exports covering 38 molecules to 18 destinations in 2023.

0
active US DMFs
0
valid CEPs
3
registered plants
6
filings across 2 regulators

Registered plants

Site FDA FEI
vadodara 391 440, India Not on file
Vadodara, India Not on file
vadodara 391 440, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) 5 3
MINSA (CR) 1 None

Scale

Year Revenue Exports Destinations
2023 Not reported $3.4M 18
2022 Not reported $8.9M 22

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 We do not publish the identity of any buyer.

Questions about Oneiro Chemicals

Does Oneiro Chemicals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Oneiro Chemicals. It does have 6 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Oneiro Chemicals manufacture?
3 registered sites are on record, in India (Vadodara 391 440 and Vadodara among others). Every site is listed on this page with the register it came from.
Which regulators recognise Oneiro Chemicals'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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Comparable suppliers

Abbott Healthcare also in India Accent Pharmaceuticals Diagnostics also in India Accure Labs Pvt.Ltd also in India ACME Formulation also in India Acme Generics also in India

Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

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