Suppliers / Therapiva

Therapiva

India Updated 9 July 2026

Therapiva is an API manufacturer based in India. It appears in 1 regulatory filing across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by MFDS (Korea). Customs aggregates show $379K of exports covering 5 molecules to 2 destinations in 2022.

0
active US DMFs
0
valid CEPs
0
registered plants
1
filings across 1 regulators

What they file, and where

Molecule Regulators Docs
Ondansetron SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) 1 None
MFDS (Korea) None 2

Scale

Year Revenue Exports Destinations
2022 Not reported $379K 2

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 We do not publish the identity of any buyer.

Questions about Therapiva

Does Therapiva hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Therapiva. It does have 1 filing with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
What does Therapiva make?
1 molecule is on record against Therapiva, including Ondansetron. Each links through to that molecule's full manufacturer list.
Which regulators recognise Therapiva's GMP?
Current GMP certificates are on record from MFDS (Korea). 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