Suppliers / Doctivo Lifesciences

Doctivo Lifesciences

India Updated 9 July 2026

Doctivo Lifesciences is a finished-dose manufacturer based in India. It appears in 46 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO) and ARCSA (EC). Its GMP standing is certified by CDSCO (India). Customs aggregates show $1.1M of exports covering 65 molecules to 5 destinations in 2025.

0
active US DMFs
0
valid CEPs
2
registered plants 1 with an FDA FEI number
46
filings across 2 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026.

Registered plants

Site FDA FEI
Kangra, India 3032514730
amraiwadi roadahmedabad 380 008ahmedabad, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 25 None
ARCSA (EC) 21 None
CDSCO (India) None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $276K 2
2025 Not reported $1.1M 5
2024 Not reported $941K 5
2023 Not reported $818K 2

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 We do not publish the identity of any buyer.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