Suppliers / Dishman Carbogen Amcis

Dishman Carbogen Amcis

India DCAL.BO Updated 9 July 2026

Dishman Carbogen Amcis is a contract manufacturer based in India. It holds 11 active US drug master files across a filed portfolio of 15 molecules. Its GMP standing is certified by US FDA and EMA. Its most recent recorded inspection, by US FDA, closed on 12 June 2025 as NAI. Customs aggregates show $28.9M of exports covering 396 molecules to 49 destinations in 2025.

11
active US DMFs
0
valid CEPs
2
registered plants 2 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
2 of 2 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

  • 12 June 2025 NAI US FDA
  • 7 March 2024 VAI US FDA
  • 15 February 2019 NAI US FDA
  • 26 October 2018 VAI US FDA
  • 8 July 2016 VAI US FDA
  • 22 October 2015 VAI US FDA
  • 2 May 2013 NAI US FDA
  • 17 March 2012 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, India 3004161218
Ahmedabad, India 1000607691

What they file, and where

Molecule Regulators Docs
Bupivacaine US FDA 2
Cetylpyridinium SFDA (Saudi Arabia), US FDA 2
Pralidoxime SFDA (Saudi Arabia), US FDA 2
Ropivacaine SFDA (Saudi Arabia), US FDA 2
Bisacodyl US FDA 1
Bosentan SFDA (Saudi Arabia) 1
Cetrimide US FDA 1
Cetylpiridinium SFDA (Saudi Arabia) 1
Dimethyl SFDA (Saudi Arabia) 1
Eprosartan US FDA 1
Show all 15 molecules on file
Indigotindisulfonic Acid US FDA 1
Isosulfan Blue US FDA 1
Sodium Picosulfate US FDA 1
Sodium Picosulphate SFDA (Saudi Arabia) 1
Valganciclovir SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA None 2
EMA None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $2.6M 31
2025 $311.2M $28.9M 49
2024 $312.6M $31.6M 50
2023 $292.2M $31.3M 54

Export figures are customs aggregates. We do not publish the identity of any buyer. Revenue shown in US dollars, converted from the reported currency.

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Open risk flags

  • 1 active litigation matter is on record.
  • The most recent inspection outcome was NAI, on 12 June 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