Suppliers / Quad Lifesciences

Quad Lifesciences

India Updated 9 July 2026

Quad Lifesciences is a contract manufacturer based in India. It holds one active US drug master file and 3 valid CEPs across a filed portfolio of 3 molecules. Customs aggregates show $3.9M of exports covering 40 molecules to 8 destinations in 2025.

1
active US DMFs
3
valid CEPs
1
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
S.A.S Nagar, India Not on file

What they file, and where

Molecule Regulators Docs
Nicotine EDQM, US FDA 2
Thiocolchicoside EDQM 1
Thiocolchicoside Crystallised From Ethanol EDQM 1

Also appears on these molecule pages

Colchicine contract manufacturing Mupirocin contract manufacturing Nicotine contract manufacturing Thiocolchicoside contract manufacturing

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $2.6M 9
2025 Not reported $3.9M 8

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 We do not publish the identity of any buyer.

Questions about Quad Lifesciences

Does Quad Lifesciences hold a US DMF or a CEP?
Quad Lifesciences holds 1 active US drug master file and 3 valid CEPs. 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 Quad Lifesciences manufacture?
1 registered site is on record, in India (S.a.s Nagar). Every site is listed on this page with the register it came from.
What does Quad Lifesciences make?
3 molecules are on record against Quad Lifesciences, including Nicotine, Thiocolchicoside and Thiocolchicoside Crystallised From Ethanol. 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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Comparable suppliers

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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
Customs aggregates
Export values, molecule and destination counts