Suppliers / Vandana Life Sciences

Vandana Life Sciences

India Updated 9 July 2026

Vandana Life Sciences is an API manufacturer based in India. It holds one active US drug master file.

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

What they file, and where

Molecule Regulators Docs
Lamivudine US FDA 1

Also appears on these molecule pages

Lamivudine API

Questions about Vandana Life Sciences

Does Vandana Life Sciences hold a US DMF or a CEP?
Vandana Life Sciences 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.
What does Vandana Life Sciences make?
1 molecule is on record against Vandana Life Sciences, including Lamivudine. 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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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