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 We do not publish the identity of any buyer.

Questions about Doctivo Lifesciences

Does Doctivo Lifesciences hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Doctivo Lifesciences. It does have 46 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Doctivo Lifesciences FDA-registered?
One site operated by Doctivo Lifesciences carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
Where does Doctivo Lifesciences manufacture?
2 registered sites are on record, in India (Kangra and Amraiwadi Roadahmedabad 380 008ahmedabad). Every site is listed on this page with the register it came from.
Which regulators recognise Doctivo Lifesciences's GMP?
Current GMP certificates are on record from CDSCO (India). 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.

Comparing suppliers?

Choose your molecules and target markets. Doctivo Lifesciences comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Comparable suppliers

Abbott Healthcare also in India Accent Pharmaceuticals Diagnostics also in India Accure Labs Pvt.Ltd also in India ACME Formulation also in India Acme Generics also in India

Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

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