Suppliers / Envee Drugs

Envee Drugs

India Updated 9 July 2026

Envee Drugs is an API manufacturer based in India. It holds one active US drug master file. Its GMP standing is certified by CDSCO (India). Customs aggregates show $5.3M of exports covering 96 molecules to 14 destinations in 2025.

1
active US DMFs
0
valid CEPs
2
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
t dumral tal nadiad dumral 387 355 kheda, India Not on file
post dumraltal nadiaddumral 387 355kheda, India Not on file

What they file, and where

Molecule Regulators Docs
Clobetasol Propionate US FDA 1

Also appears on these molecule pages

Clobetasol API

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $677K 9
2025 Not reported $5.3M 14
2024 Not reported $3.5M 16
2023 Not reported $3.3M 18

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 We do not publish the identity of any buyer.

Questions about Envee Drugs

Does Envee Drugs hold a US DMF or a CEP?
Envee Drugs holds 1 active US drug master file. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Where does Envee Drugs manufacture?
2 registered sites are on record, in India (T Dumral Tal Nadiad Dumral 387 355 Kheda and Post Dumraltal Nadiaddumral 387 355kheda). Every site is listed on this page with the register it came from.
What does Envee Drugs make?
1 molecule is on record against Envee Drugs, including Clobetasol Propionate. Each links through to that molecule's full manufacturer list.
Which regulators recognise Envee Drugs'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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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