Suppliers / Curia India

Curia India

India Updated 9 July 2026

The public registers hold a second record for Curia India. The fuller profile, with 116 active US DMFs and 8 valid CEPs, is at Curia. Figures on this page cover only this record.

Curia India is an API manufacturer based in India. It holds one active US drug master file. Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 16 February 2024 as VAI. Customs aggregates show $17.4M of exports covering 194 molecules to 21 destinations in 2025.

1
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 16 February 2024 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Aurangabad, India 3008580576

What they file, and where

Molecule Regulators Docs
Furosemide US FDA 1

Also appears on these molecule pages

Furosemide API

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $1.1M 6
2025 Not reported $17.4M 21
2024 Not reported $14.9M 27
2023 Not reported $18.5M 18

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 We do not publish the identity of any buyer.

Questions about Curia India

Does Curia India hold a US DMF or a CEP?
Curia India holds 1 active US drug master file. 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.
Is Curia India FDA-registered?
One site operated by Curia India carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Curia India's last inspection go?
The most recent inspection on record closed on 16 February 2024 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 1 inspection is on file.
Where does Curia India manufacture?
1 registered site is on record, in India (Aurangabad). Every site is listed on this page with the register it came from.
What does Curia India make?
1 molecule is on record against Curia India, including Furosemide. Each links through to that molecule's full manufacturer list.
Which regulators recognise Curia India's GMP?
Current GMP certificates are on record from US FDA. 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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Open risk flags

  • The most recent inspection outcome was VAI, on 16 February 2024.

Comparable suppliers

Ipca Laboratories shares 1 molecule EUROAPI shares 1 molecule F.I.S. Fabbrica Italiana Sintetici shares 1 molecule Kalintis Healthcare shares 1 molecule Ambition Pharma shares 1 molecule

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