Suppliers / Virdev Intermediates

Virdev Intermediates

India Updated 9 July 2026

Virdev Intermediates is an API and finished-dose manufacturer based in India. It holds one active US drug master file and one valid CEP across a filed portfolio of 4 molecules. Its GMP standing is certified by EMA and CDSCO (India). Customs aggregates show $23K of exports covering 1 molecule to 1 destination in 2025.

1
active US DMFs
1
valid CEPs
3
registered plants 1 with an FDA FEI number
7
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Surat, India 3033605590
Surat, India Not on file
Surat, India Not on file

What they file, and where

Molecule Regulators Docs
Lymecycline EDQM 1
Sugammadex SFDA (Saudi Arabia) 1
Vardenafil SFDA (Saudi Arabia) 1
Vonoprazan US FDA 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) 7 2
EMA None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $21K 1
2025 Not reported $23K 1
2024 Not reported $112K 2
2023 Not reported $39K 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 We do not publish the identity of any buyer.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