Suppliers / BDR Lifesciences

BDR Lifesciences

India Updated 9 July 2026

BDR Lifesciences is a finished-dose manufacturer based in India. It holds 10 active US drug master files and 2 valid CEPs across a filed portfolio of 8 molecules. Its filings concentrate with CDSCO (India) and JFDA (JO). Its GMP standing is certified by CDSCO (India) and EMA. Customs aggregates show $27K of exports covering 2 molecules to 1 destination in 2025.

10
active US DMFs
2
valid CEPs
4
registered plants 1 with an FDA FEI number
21
filings across 2 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Vadodara, India 3009119873
Luna Village, India Not on file
taluka padra luna 391 440 vadodara, India Not on file
taluka padraluna 391 440vadodara, India Not on file

What they file, and where

Molecule Regulators Docs
Avatrombopag US FDA 2
Enzalutamide US FDA 2
Nintedanib US FDA 2
Olaparib US FDA 2
Relugolix US FDA 2
Sorafenib EDQM, SFDA (Saudi Arabia) 2
Lapatinib Ditosylate SFDA (Saudi Arabia) 1
Pemetrexed Disodium EDQM 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) 20 2
JFDA (JO) 1 None
EMA None 2

Scale

Year Revenue Exports Destinations
2025 Not reported $27K 1
2024 Not reported $28K 1
2023 Not reported $8K 1

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 We do not publish the identity of any buyer.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