Suppliers / Cipla

Cipla

India CIPLA.NS 419 employees 3 duplicate records merged Updated 9 July 2026

Cipla is an API and finished-dose manufacturer based in India. It holds 161 active US drug master files and 272 valid CEPs. Its filings concentrate with SAHPRA (ZA), US FDA and ARCSA (EC). Its GMP standing is certified by EMA, CDSCO (India) and ANVISA (Brazil), among 12 authorities. Its most recent recorded inspection, by US FDA, closed on 30 May 2025 as VAI. Customs aggregates show $1.0B of exports covering 18,463 molecules to 132 destinations in 2025.

161
active US DMFs
272
valid CEPs
12
registered plants 4 with an FDA FEI number
2,570
filings across 34 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
4 of 4 confirmed
Inspections
6 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

  • 30 May 2025 VAI US FDA
  • 13 November 2024 VAI US FDA
  • 21 June 2024 VAI US FDA
  • 8 May 2024 VAI US FDA
  • 4 April 2024 VAI US FDA
  • 17 February 2023 OAI US FDA
  • 26 August 2022 OAI US FDA
  • 31 January 2020 VAI US FDA

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

Registered plants

Site FDA FEI
Indore, United Arab Emirates Not on file
Verna, United Arab Emirates Not on file
Baddi, Colombia Not on file
Verna, Colombia Not on file
ADDLESTONE, United Kingdom Not on file
Bengaluru, India 3002806691

6 further sites are on record.

What they file, and where

Molecule Regulators Docs
Fluticasone Propionate EDQM, SFDA (Saudi Arabia), US FDA 21
Omeprazole EDQM, SFDA (Saudi Arabia), US FDA 16
Mometasone Furoate EDQM, SFDA (Saudi Arabia), US FDA 12
Amlodipine EDQM, SFDA (Saudi Arabia), US FDA 10
Budesonide EDQM, SFDA (Saudi Arabia), US FDA 10
Salbutamol Sulfate EDQM 8
Venlafaxine Hydrochloride EDQM 8
Celecoxib EDQM, SFDA (Saudi Arabia), US FDA 7
Albuterol EDQM, US FDA 6
Escitalopram EDQM, US FDA 6
Show all 30 molecules on file
Esomeprazole EDQM, US FDA 6
Etoposide EDQM, SFDA (Saudi Arabia), US FDA 6
Finasteride EDQM, SFDA (Saudi Arabia), US FDA 6
Fluconazole EDQM, SFDA (Saudi Arabia), US FDA 6
Granisetron EDQM, US FDA 6
Letrozole EDQM, SFDA (Saudi Arabia), US FDA 6
Meloxicam EDQM, SFDA (Saudi Arabia), US FDA 6
Ondansetron EDQM, SFDA (Saudi Arabia), US FDA 6
Pantoprazole EDQM, SFDA (Saudi Arabia), US FDA 6
Risperidone EDQM, SFDA (Saudi Arabia), US FDA 6
Rivastigmine EDQM, SFDA (Saudi Arabia), US FDA 6
Sorafenib EDQM, US FDA 6
Carvedilol EDQM, SFDA (Saudi Arabia) 5
Citalopram EDQM, US FDA 5
Entecavir EDQM, US FDA 5
Exemestane EDQM, US FDA 5
Felodipine EDQM, US FDA 5
Formoterol EDQM, US FDA 5
Gefitinib EDQM, US FDA 5
Lamivudine EDQM, US FDA 5

Also appears on these molecule pages

Show 111 more molecule pages
Capecitabine finished dose Carboplatin API Carvedilol API Celecoxib API Cephalexin finished dose Cetirizine API Ciclopirox finished dose Ciclosporin finished dose Citalopram API Clavulanic Acid finished dose Clotrimazole finished dose Dapagliflozin finished dose Daptomycin finished dose Desloratadine API Diltiazem finished dose Dolutegravir API Drospirenone finished dose Dutasteride finished dose Empagliflozin API Emtricitabine API Ertapenem finished dose Escitalopram API Esomeprazole API Felodipine API Fenofibrate finished dose Fexofenadine finished dose Finasteride API Fluconazole API Fluorometholone finished dose Fluticasone API Formoterol API Gabapentin finished dose Gatifloxacin finished dose Glibenclamide finished dose Gliclazide finished dose Hydrochlorothiazide finished dose Hydrocortisone finished dose Irbesartan finished dose Isoniazid finished dose Isotretinoin finished dose Itraconazole finished dose Ketoconazole finished dose Lamivudine API Lamotrigine API Lansoprazole API Latanoprost finished dose Lenalidomide API Letrozole API Levocetirizine API Levofloxacin API Levonorgestrel API Linagliptin finished dose Liraglutide finished dose Lisinopril finished dose Lorazepam finished dose Mebendazole API Meloxicam API Meprobamate finished dose Mirabegron API Mometasone API Montelukast API Moxifloxacin finished dose Nifedipine finished dose Ofloxacin finished dose Omeprazole API Ondansetron API Oxcarbazepine finished dose Paclitaxel finished dose Pantoprazole API Pioglitazone API Pramipexole API Praziquantel API Pregabalin finished dose Prucalopride finished dose Quetiapine finished dose Ramipril API Risperidone API Ritonavir API Rivaroxaban API Rosuvastatin finished dose Salbutamol API Salmeterol API Saxagliptin finished dose Sertraline finished dose Sildenafil finished dose Sitagliptin finished dose Solifenacin API Sulbactam finished dose Sulfamethoxazole finished dose Sumatriptan finished dose Tacrolimus finished dose Tadalafil finished dose Tamoxifen finished dose Tamsulosin API Telmisartan API Tenofovir Disoproxil API Terbinafine API Testosterone finished dose Tetracycline finished dose Tiotropium API Topiramate API Trimetazidine API Umeclidinium API Valaciclovir API Valacyclovir API Valproic Acid finished dose Vigabatrin finished dose Vilanterol API Vildagliptin finished dose Zolmitriptan finished dose Venlafaxine API

Filings and GMP by regulator

Regulator Filings GMP certificates
SAHPRA (ZA) 912 3
US FDA 314 5
ARCSA (EC) 180 None
DIGEMAPS (DO) 143 None
EMA 103 20
ZAMRA (ZM) 84 None
CDSCO (India) None 19
ANVISA (Brazil) None 6
MHRA (UK) None 5
TMDA (TZ) None 3
NAFDAC (NG) None 3
MFDS (Korea) None 2
FDA (GH) None 2
NCELS (KZ) None 1
INVIMA (CO) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $118.8M 81
2025 $3.2B $1.0B 132
2024 $3.1B $744.1M 127
2023 $2.8B $766.9M 135

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

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Open risk flags

  • 71 active litigation matters are on record.
  • One recent serious compliance event is on record.
  • The most recent inspection outcome was VAI, on 30 May 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