Suppliers / Orchid Pharma

Orchid Pharma

India ORCHPHARMA.BO 64 employees Updated 9 July 2026

Orchid Pharma is an API manufacturer based in India. It holds 42 active US drug master files and 15 valid CEPs. Its filings concentrate with CDSCO (India), US FDA and MINSA (CR). Its GMP standing is certified by EMA, MFDS (Korea) and US FDA. Its most recent recorded inspection, by US FDA, closed on 18 February 2025 as VAI. Customs aggregates show $73.7M of exports covering 633 molecules to 50 destinations in 2025.

42
active US DMFs
15
valid CEPs
3
registered plants 1 with an FDA FEI number
5
filings across 3 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
5 of 5 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Inspection history

  • 18 February 2025 VAI US FDA
  • 30 July 2019 VAI US FDA
  • 4 September 2015 VAI US FDA
  • 20 August 2012 VAI US FDA
  • 23 September 2010 VAI US FDA

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

Registered plants

Site FDA FEI
Chennai, India Not on file
Alathur, India Not on file
Chengalpattu, India 3003747558

What they file, and where

Molecule Regulators Docs
Ceftazidime EDQM, SFDA (Saudi Arabia), US FDA 6
Cefuroxime US FDA 4
Cefazolin EDQM, US FDA 3
Cefepime US FDA 3
Cefotaxime EDQM, SFDA (Saudi Arabia), US FDA 3
Ceftriaxone EDQM, SFDA (Saudi Arabia), US FDA 3
Avibactam SFDA (Saudi Arabia), US FDA 2
Cefadroxil EDQM, US FDA 2
Cefixime EDQM, US FDA 2
Cefprozil SFDA (Saudi Arabia), US FDA 2
Show all 30 molecules on file
Cefuroxime Axetil EDQM 2
Cefuroxime Sodium Sterile EDQM 2
7-Aminodesacetoxycephalosporanic Acid US FDA 1
Alendronic Acid US FDA 1
Almotriptan US FDA 1
Armodafinil US FDA 1
Carbonate Ion US FDA 1
Cefalexin Monohydrate EDQM 1
Cefdinir US FDA 1
Cefditoren US FDA 1
Cefepime Dihydrochloride EDQM 1
Cefoxitin US FDA 1
Cefoxitin Sodium EDQM 1
Cefpodoxime US FDA 1
Cefradine EDQM 1
Ceftazidime Pentahydrate With Sodium Carbonate For Injection EDQM 1
Cephalexin US FDA 1
Clopidogrel US FDA 1
Dexlansoprazole US FDA 1
Dipyridamole US FDA 1

Also appears on these molecule pages

Show 3 more molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) 3 None
US FDA 1 1
MINSA (CR) 1 None
EMA None 3
MFDS (Korea) None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $10.6M 27
2025 Not reported $73.7M 50
2024 $96.9M $86.0M 48
2023 $111.7M $82.5M 50
2022 $104.2M Not reported Not reported

Export figures are customs aggregates. We do not publish the identity of any buyer. Revenue shown in US dollars, converted from the reported currency.

Comparing suppliers?

Choose your molecules and target markets. Orchid Pharma comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Open risk flags

  • 3 active litigation matters are on record.
  • The most recent inspection outcome was VAI, on 18 February 2025.

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
Company filings
Revenue as reported