Suppliers / Seutic Labs

Seutic Labs

India Updated 9 July 2026

Seutic Labs is an API manufacturer based in India. Its GMP standing is certified by CDSCO (India).

0
active US DMFs
0
valid CEPs
2
registered plants 1 with an FDA FEI number
0
filings across 0 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
Bidar, India Not on file
Bidar District, India 3017299509

What they file, and where

Molecule Regulators Docs
Favipiravir SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Favipiravir API

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) None 2

Questions about Seutic Labs

Is Seutic Labs FDA-registered?
One site operated by Seutic Labs 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 Seutic Labs manufacture?
2 registered sites are on record, in India (Bidar and Bidar District). Every site is listed on this page with the register it came from.
What does Seutic Labs make?
1 molecule is on record against Seutic Labs, including Favipiravir. Each links through to that molecule's full manufacturer list.
Which regulators recognise Seutic Labs'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.

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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