Suppliers / BDR Lifesciences

BDR Lifesciences

India reconciled across 17 public records · 8 entities Updated 9 July 2026

BDR Lifesciences is a finished-dose manufacturer based in India. It holds 5 active US drug master files and 2 valid CEPs across a filed portfolio of 8 molecules. Its filings concentrate with CDSCO (India), DIGEMAPS (DO) and MINSA (CR). Its GMP standing is certified by CDSCO (India), EMA and EDQM, among 4 authorities. Customs aggregates show $27K of exports covering 2 molecules to 1 destination in 2025.

5
active US DMFs
2
valid CEPs
17
registered plants 5 with an FDA FEI number
182
filings across 9 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
Vadodara, India 3010166818
Vadodara, India 3038848101
VADODARA, India Not on file

11 further sites are on record.

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) 67 13
DIGEMAPS (DO) 53 None
MINSA (CR) 24 None
ARCSA (EC) 15 None
NCELS (KZ) 7 None
ANPP (DZ) 6 None
EMA None 5
EDQM None 2
ANVISA (Brazil) None 1

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 We do not publish the identity of any buyer.

Questions about BDR Lifesciences

Does BDR Lifesciences hold a US DMF or a CEP?
BDR Lifesciences holds 5 active US drug master files and 2 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 BDR Lifesciences FDA-registered?
5 sites operated by BDR Lifesciences 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.
Where does BDR Lifesciences manufacture?
17 registered sites are on record, in India (Vadodara, Luna Village and Taluka Padra Luna 391 440 Vadodara among others). Every site is listed on this page with the register it came from.
What does BDR Lifesciences make?
8 molecules are on record against BDR Lifesciences, including Sorafenib, Avatrombopag, Enzalutamide and Lapatinib Ditosylate. Each links through to that molecule's full manufacturer list.
Which regulators recognise BDR Lifesciences's GMP?
Current GMP certificates are on record from CDSCO (India), EMA, EDQM and ANVISA (Brazil). 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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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