Suppliers / Cadila Pharmaceuticals

Cadila Pharmaceuticals

India 2 duplicate records merged Updated 9 July 2026

Cadila Pharmaceuticals is an API and finished-dose manufacturer based in India. It holds 28 active US drug master files and 18 valid CEPs. Its filings concentrate with US FDA, PPB (KE) and DAV (Vietnam). Its GMP standing is certified by CDSCO (India), EMA and US FDA, among 6 authorities. Its most recent recorded inspection, by US FDA, closed on 26 September 2025 as NAI. Customs aggregates show $47.2M of exports covering 686 molecules to 66 destinations in 2025.

28
active US DMFs
18
valid CEPs
12
registered plants 3 with an FDA FEI number
403
filings across 15 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
3 of 3 confirmed
Inspections
8 of 8 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

  • 26 September 2025 NAI US FDA
  • 10 May 2024 VAI US FDA
  • 7 April 2023 NAI US FDA
  • 17 June 2022 NAI US FDA
  • 14 February 2020 NAI US FDA
  • 9 August 2019 VAI US FDA
  • 3 May 2018 VAI US FDA
  • 13 February 2018 VAI US FDA

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

Registered plants

Site FDA FEI
Ahmedabad, United Arab Emirates Not on file
AHMEDABAD, India Not on file
ankleshwar 393 002 bharuch, India Not on file
Plot No., India Not on file
sad road dholka dholka 387 810 ahmedabad, India Not on file
narodaahme dabad 382 330ahmedabad, India Not on file

6 further sites are on record.

What they file, and where

Molecule Regulators Docs
Celecoxib EDQM, SFDA (Saudi Arabia), US FDA 4
Desloratadine EDQM, SFDA (Saudi Arabia), US FDA 3
Fluoxetine EDQM, SFDA (Saudi Arabia), US FDA 3
Loratadine EDQM, SFDA (Saudi Arabia), US FDA 3
Nebivolol EDQM, SFDA (Saudi Arabia), US FDA 3
Olanzapine EDQM, SFDA (Saudi Arabia), US FDA 3
Ondansetron EDQM, SFDA (Saudi Arabia), US FDA 3
Venlafaxine EDQM, US FDA 3
Amlodipine EDQM, US FDA 2
Aripiprazole EDQM, US FDA 2
Show all 30 molecules on file
Carvedilol EDQM, US FDA 2
Chlorhexidine US FDA 2
Sildenafil EDQM, US FDA 2
Amlodipin SFDA (Saudi Arabia) 1
Atomoxetine US FDA 1
Atorvastatin US FDA 1
Bosentan US FDA 1
Bupropion US FDA 1
Escitalopram US FDA 1
Ethambutol US FDA 1
Glyburide US FDA 1
Hydralazine US FDA 1
Nateglinide US FDA 1
Olmesartan US FDA 1
Olmesartan Medoxomil EDQM 1
Paliperidone US FDA 1
Raloxifene US FDA 1
Rivaroxaban EDQM 1
Rupatadine Fumarate EDQM 1
Sodium Alendronate EDQM 1

Also appears on these molecule pages

Show 56 more molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA 73 2
PPB (KE) 63 None
DAV (Vietnam) 59 None
ZAMRA (ZM) 55 None
UZPHARM (UZ) 35 None
NAFDAC (NG) 31 1
CDSCO (India) None 11
EMA None 6
FDA (GH) None 1
MHRA (UK) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $18.0M 73
2025 Not reported $47.2M 66
2024 Not reported $57.5M 60
2023 Not reported $83.9M 67

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

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Open risk flags

  • 2 active litigation matters are on record.
  • The most recent inspection outcome was NAI, on 26 September 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