Suppliers / Alivus Life Sciences

Alivus Life Sciences

India ALIVUS.NS 590 employees 2 duplicate records merged Updated 9 July 2026

Alivus Life Sciences is an API manufacturer based in India. It holds 272 active US drug master files and 43 valid CEPs. Its GMP standing is certified by US FDA and EMA. Its most recent recorded inspection, by US FDA, closed on 30 May 2025 as NAI. Customs aggregates show $58.5M of exports covering 903 molecules to 62 destinations in 2025.

272
active US DMFs
43
valid CEPs
4
registered plants 3 with an FDA FEI number
2
filings across 1 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

  • 30 May 2025 NAI US FDA
  • 31 January 2025 VAI US FDA
  • 5 July 2019 VAI US FDA
  • 26 October 2018 NAI US FDA
  • 16 December 2016 VAI US FDA
  • 17 April 2015 VAI US FDA
  • 27 February 2015 VAI US FDA
  • 15 October 2011 VAI US FDA

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

Registered plants

Site FDA FEI
Mumbai, India Not on file
Bharuch, India 3007514214
Ankleshwar, India 3004006229
Solapur, India 3014026060

What they file, and where

Molecule Regulators Docs
Esomeprazole EDQM, US FDA 9
Rosuvastatin EDQM, US FDA 7
Atovaquone EDQM, US FDA 6
Ezetimibe US FDA 6
Sitagliptin US FDA 6
Aprepitant EDQM, US FDA 5
Tadalafil EDQM, US FDA 5
Telmisartan EDQM, US FDA 5
Terbinafine EDQM, US FDA 5
Zolpidem EDQM, US FDA 5
Show all 30 molecules on file
Bupropion US FDA 4
Desloratadine EDQM, US FDA 4
Fluconazole EDQM, US FDA 4
Glimepiride EDQM, US FDA 4
Linezolid US FDA 4
Sucralfate US FDA 4
Tafamidis US FDA 4
Zonisamide US FDA 4
Adapalene EDQM, US FDA 3
Amiodarone EDQM, US FDA 3
Brivaracetam EDQM, US FDA 3
Deferasirox EDQM, US FDA 3
Dipyridamole EDQM, US FDA 3
Fingolimod EDQM, US FDA 3
Lacosamide EDQM, US FDA 3
Mirabegron EDQM, US FDA 3
Perindopril SFDA (Saudi Arabia), US FDA 3
Pirfenidone EDQM, US FDA 3
Rivaroxaban EDQM, US FDA 3
Rizatriptan EDQM, US FDA 3

Also appears on these molecule pages

Show 96 more molecule pages
Brivaracetam API Bupropion API Carvedilol API Choline Fenofibrate API Cilostazol API Dabigatran Etexilate API Daclatasvir API Dapagliflozin API Darifenacin API Deferasirox API Desloratadine API Deucravacitinib API Dimethyl API Dipyridamole API Dronedarone API Efinaconazole API Elagolix API Enzalutamide API Esomeprazole API Eszopiclone API Ezetimibe API Finerenone API Fingolimod API Fluconazole API Fluvoxamine API Fosaprepitant API Glimepiride API Hydralazine API Imiquimod API Isavuconazonium API Itraconazole API Ivacaftor API Labetalol API Lacosamide API Lasmiditan API Levocetirizine API Lifitegrast API Linagliptin API Linezolid API Lithium Carbonate API Loratadine API Lurasidone API Milnacipran API Mirabegron API Nintedanib API Olaparib API Olmesartan API Olmesartan Medoxomil API Olopatadine API Omeprazole API Ondansetron API Ospemifene API Palbociclib API Paliperidone API Perindopril API Perindopril Tert-Butylamine API Pirfenidone API Prasugrel API Pregabalin API Proguanil API Propranolol API Raloxifene API Ranolazine API Rasagiline API Relugolix API Riluzole API Rivaroxaban API Rizatriptan API Roflumilast API Ropinirole API Rosuvastatin API Rufinamide API Ruxolitinib API Saxagliptin API Solifenacin API Sucralfate API Tadalafil API Tafamidis API Tavaborole API Tazarotene API Telmisartan API Terbinafine API Teriflunomide API Tofacitinib API Topiramate API Trospium API Ursodeoxycholic Acid API Verapamil API Vibegron API Vilazodone API Viloxazine API Voriconazole API Zolmitriptan API Zolpidem API Zonisamide API Sitagliptin API

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 2 None
US FDA None 2
EMA None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $10.7M 50
2025 Not reported $58.5M 62
2021 $255.0M 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.

Questions about Alivus Life Sciences

Does Alivus Life Sciences hold a US DMF or a CEP?
Alivus Life Sciences holds 272 active US drug master files and 43 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 Alivus Life Sciences FDA-registered?
3 sites operated by Alivus Life Sciences 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 Alivus Life Sciences's last inspection go?
The most recent inspection on record closed on 30 May 2025 as NAI (No Action Indicated: nothing objectionable was found). 8 inspections are on file.
Where does Alivus Life Sciences manufacture?
4 registered sites are on record, in India (Mumbai, Bharuch and Ankleshwar among others). Every site is listed on this page with the register it came from.
What does Alivus Life Sciences make?
30 molecules are on record against Alivus Life Sciences, including Esomeprazole, Rosuvastatin, Atovaquone and Ezetimibe. Each links through to that molecule's full manufacturer list.
Which regulators recognise Alivus Life Sciences's GMP?
Current GMP certificates are on record from US FDA and EMA. 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 NAI, 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