Suppliers / Psychotropics India

Psychotropics India

India 3 duplicate records merged Updated 9 July 2026

Psychotropics India is a finished-dose manufacturer based in India. It appears in 77 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with EFDA (ET), NAFDAC (NG) and DAV (Vietnam). Its GMP standing is certified by NAFDAC (NG) and ANVISA (Brazil). Customs aggregates show $7.7M of exports covering 1,208 molecules to 29 destinations in 2025.

0
active US DMFs
0
valid CEPs
2
registered plants
77
filings across 5 regulators

Registered plants

Site FDA FEI
HARIDWAR, India Not on file
Uttarkhand, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EFDA (ET) 52 None
NAFDAC (NG) 19 2
DAV (Vietnam) 3 None
TMDA (TZ) 2 None
ZAMRA (ZM) 1 None
ANVISA (Brazil) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $1.1M 10
2025 Not reported $7.7M 29
2024 Not reported $6.3M 29
2023 Not reported $6.1M 33

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 We do not publish the identity of any buyer.

Questions about Psychotropics India

Does Psychotropics India hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Psychotropics India. It does have 77 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Psychotropics India manufacture?
2 registered sites are on record, in India and Nigeria (Haridwar and Uttarkhand). Every site is listed on this page with the register it came from.
Which regulators recognise Psychotropics India's GMP?
Current GMP certificates are on record from NAFDAC (NG) 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