Suppliers / Cdymax (India) Pharma

Cdymax (India) Pharma

India 267 employees Updated 9 July 2026

Cdymax (India) Pharma is an API manufacturer based in India. It holds 17 active US drug master files and 5 valid CEPs across a filed portfolio of 19 molecules. Its GMP standing is certified by EMA. Customs aggregates show $18.6M of exports covering 237 molecules to 28 destinations in 2025.

17
active US DMFs
5
valid CEPs
1
registered plants
12
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Bangalore, India Not on file

What they file, and where

Molecule Regulators Docs
Imatinib Mesilate EDQM 3
Palbociclib SFDA (Saudi Arabia), US FDA 3
Capecitabine EDQM, US FDA 2
Dasatinib US FDA 2
Enzalutamide SFDA (Saudi Arabia), US FDA 2
Erlotinib US FDA 2
Pazopanib SFDA (Saudi Arabia), US FDA 2
Sunitinib SFDA (Saudi Arabia), US FDA 2
Abiraterone US FDA 1
Atazanavir US FDA 1
Show all 19 molecules on file
Efavirenz US FDA 1
Gefitinib US FDA 1
Ibrutinib US FDA 1
Olaparib US FDA 1
Pabrolib SFDA (Saudi Arabia) 1
Pemetrexed US FDA 1
Pemetrexed Disodium EDQM 1
Pemetrexed Disodium Hemipentahydrate SFDA (Saudi Arabia) 1
Tenofovir Disoproxil US FDA 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 12 None
EMA None 4

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $3.3M 15
2025 Not reported $18.6M 28
2024 Not reported $21.3M 32
2023 Not reported $21.1M 26

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 We do not publish the identity of any buyer.

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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