Suppliers / Cadila Pharmaceuticals

Cadila Pharmaceuticals

India reconciled across 14 public records · 10 entities Updated 9 July 2026

Cadila Pharmaceuticals is an API and finished-dose manufacturer based in India. It holds 32 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.

32
active US DMFs
18
valid CEPs
20
registered plants 3 with an FDA FEI number
405
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
  • 25 July 2016 OAI US FDA
  • 15 May 2015 VAI US FDA
  • 28 March 2014 OAI US FDA
  • 21 September 2012 NAI 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
Gelan, Ethiopia 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

14 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 33 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
Valsartan US FDA 1
Venlafaxine Hydrochloride EDQM 1
Zolpidem EDQM 1

Also appears on these molecule pages

Show 78 more molecule pages
Cefixime finished dose Cefoperazone finished dose Cefotaxime finished dose Cefpodoxime finished dose Ceftriaxone finished dose Cefuroxime finished dose Celecoxib API Cephalexin finished dose Cetirizine finished dose Chlorhexidine API Chlorphenamine finished dose Chlorpheniramine finished dose Ciprofloxacin finished dose Clopidogrel finished dose Desloratadine API Dexamethasone finished dose Domperidone finished dose Donepezil finished dose Enalapril finished dose Erythromycin finished dose Escitalopram API Etoricoxib finished dose Ferrous finished dose Fexofenadine finished dose Fluconazole finished dose Fluoxetine API Glibenclamide API Glimepiride finished dose Glyburide API Hydralazine API Isoniazid finished dose Ketorolac Tromethamine finished dose Labetalol finished dose Levofloxacin finished dose Loratadine API Losartan finished dose Mebendazole finished dose Meloxicam finished dose Metronidazole finished dose Mirtazapine finished dose Montelukast finished dose Nateglinide API Nebivolol API Neomycin finished dose Nifedipine finished dose Ofloxacin finished dose Olanzapine API Olmesartan API Olmesartan Medoxomil API Ondansetron API Paliperidone API Palonosetron finished dose Pantoprazole finished dose Paroxetine finished dose Pioglitazone finished dose Pregabalin finished dose Rabeprazole finished dose Raloxifene API Ranitidine finished dose Rivaroxaban API Rivastigmine finished dose Rosuvastatin finished dose Rupatadine API Sildenafil API Sodium Alendronate API Sulfamethoxazole finished dose Tadalafil finished dose Telmisartan finished dose Timolol finished dose Tinidazole finished dose Tizanidine finished dose Triamcinolone finished dose Triamcinolone Acetonide finished dose Valsartan API Venlafaxine API Vildagliptin finished dose Xylometazoline finished dose Zolpidem API

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 2
CDSCO (India) None 15
EMA None 6
MHRA (UK) None 1
FDA (GH) 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.

Questions about Cadila Pharmaceuticals

Does Cadila Pharmaceuticals hold a US DMF or a CEP?
Cadila Pharmaceuticals holds 32 active US drug master files and 18 valid CEPs. 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 Cadila Pharmaceuticals FDA-registered?
3 sites operated by Cadila Pharmaceuticals carry an FDA establishment identifier (FEI), which means they are registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Cadila Pharmaceuticals's last inspection go?
The most recent inspection on record closed on 26 September 2025 as NAI (No Action Indicated: nothing objectionable was found). 13 inspections are on file, of which 2 closed as OAI.
Where does Cadila Pharmaceuticals manufacture?
20 registered sites are on record, in United Arab Emirates, Ethiopia, India and Nigeria (Ahmedabad, Gelan and Ahmedabad among others). Every site is listed on this page with the register it came from.
What does Cadila Pharmaceuticals make?
33 molecules are on record against Cadila Pharmaceuticals, including Celecoxib, Desloratadine, Fluoxetine and Loratadine. Each links through to that molecule's full manufacturer list.
Which regulators recognise Cadila Pharmaceuticals's GMP?
Current GMP certificates are on record from CDSCO (India), EMA, US FDA, NAFDAC (NG), MHRA (UK) and 1 more. 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

  • 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