Suppliers / Vannsh Life Sciences

Vannsh Life Sciences

India Updated 9 July 2026

Vannsh Life Sciences is an API manufacturer based in India. It holds 2 active US drug master files across a filed portfolio of 2 molecules. Customs aggregates show $408K of exports covering 25 molecules to 7 destinations in 2025.

2
active US DMFs
0
valid CEPs
1
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
Visakhapatnam, India 3021138307

What they file, and where

Molecule Regulators Docs
Capecitabine US FDA 1
Carmustine US FDA 1

Also appears on these molecule pages

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $113K 1
2025 Not reported $408K 7

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 We do not publish the identity of any buyer.

Questions about Vannsh Life Sciences

Does Vannsh Life Sciences hold a US DMF or a CEP?
Vannsh Life Sciences holds 2 active US drug master files. 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.
Is Vannsh Life Sciences FDA-registered?
One site operated by Vannsh Life Sciences 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 Vannsh Life Sciences manufacture?
1 registered site is on record, in India (Visakhapatnam). Every site is listed on this page with the register it came from.
What does Vannsh Life Sciences make?
2 molecules are on record against Vannsh Life Sciences, including Capecitabine and Carmustine. Each links through to that molecule's full manufacturer list.

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
Customs aggregates
Export values, molecule and destination counts