Suppliers / Ipca Laboratories

Ipca Laboratories

India IPCALAB.NS Updated 9 July 2026

Ipca Laboratories is an API and finished-dose manufacturer based in India. It holds 52 active US drug master files and 132 valid CEPs. Its filings concentrate with MHRA (UK), US FDA and TMDA (TZ). Its GMP standing is certified by CDSCO (India), MHRA (UK) and EMA, among 6 authorities. Its most recent recorded inspection, by US FDA, closed on 5 December 2025 as VAI. Customs aggregates show $348.3M of exports covering 9,744 molecules to 137 destinations in 2025.

52
active US DMFs
132
valid CEPs
12
registered plants 3 with an FDA FEI number
465
filings across 19 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
3 of 3 confirmed
Inspections
5 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

  • 5 December 2025 VAI US FDA
  • 23 June 2023 VAI US FDA
  • 13 June 2023 VAI US FDA
  • 26 April 2023 VAI US FDA
  • 20 September 2019 VAI US FDA
  • 23 August 2019 OAI US FDA
  • 4 November 2016 NAI US FDA
  • 6 October 2016 VAI US FDA

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

Registered plants

Site FDA FEI
Silvassa, United Arab Emirates Not on file
SUNDERLAND, United Kingdom Not on file
Mumbai, India Not on file
PITHAMPUR, India Not on file
GANDHIDHARN-KUTCH, India Not on file
Kutch, India Not on file

6 further sites are on record.

What they file, and where

Molecule Regulators Docs
Hydrochlorothiazide EDQM, SFDA (Saudi Arabia), US FDA 9
Metoprolol EDQM, US FDA 7
Ondansetron EDQM, SFDA (Saudi Arabia), US FDA 6
Furosemide EDQM, SFDA (Saudi Arabia), US FDA 5
Hydroxychloroquine EDQM, SFDA (Saudi Arabia), US FDA 5
Mesalazine EDQM, US FDA 5
Telmisartan EDQM, US FDA 5
Carvedilol EDQM, SFDA (Saudi Arabia), US FDA 4
Chlorthalidone EDQM, US FDA 4
Etodolac EDQM, US FDA 4
Show all 30 molecules on file
Hydroxyzine EDQM, US FDA 4
Losartan Potassium EDQM 4
Metformin EDQM, SFDA (Saudi Arabia), US FDA 4
Metoclopramide EDQM, SFDA (Saudi Arabia), US FDA 4
Propranolol EDQM, SFDA (Saudi Arabia), US FDA 4
Allopurinol EDQM, US FDA 3
Atenolol EDQM, US FDA 3
Atovaquone EDQM, US FDA 3
Bisoprolol EDQM, US FDA 3
Chloroquine EDQM, US FDA 3
Duloxetine EDQM, US FDA 3
Famotidine EDQM, SFDA (Saudi Arabia) 3
Fluoxetine EDQM, US FDA 3
Glimepiride EDQM, US FDA 3
Indapamide EDQM, SFDA (Saudi Arabia) 3
Meloxicam EDQM, US FDA 3
Olanzapine EDQM, US FDA 3
Paroxetine EDQM, SFDA (Saudi Arabia) 3
Proguanil EDQM, US FDA 3
Pyrantel EDQM, US FDA 3

Also appears on these molecule pages

Show 49 more molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
MHRA (UK) 112 6
US FDA 76 3
TMDA (TZ) 42 None
DAV (Vietnam) 41 None
EMA 36 5
MCAZ (ZW) 24 None
CDSCO (India) None 10
FDA (GH) None 4
NAFDAC (NG) None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $56.2M 96
2025 $1.0B $348.3M 137
2024 $918.7M $329.8M 132
2023 $754.7M $336.7M 136

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

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Open risk flags

  • 6 active litigation matters are on record.
  • The most recent inspection outcome was VAI, on 5 December 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