Suppliers / Nectar Lifesciences

Nectar Lifesciences

India NECLIFE.BO 2 duplicate records merged Updated 9 July 2026

Nectar Lifesciences is an API manufacturer based in India. It holds 16 active US drug master files across a filed portfolio of 9 molecules. Its filings concentrate with ARCSA (EC), ZAMRA (ZM) and EFDA (ET). Customs aggregates show $43.8M of exports covering 556 molecules to 53 destinations in 2025.

16
active US DMFs
0
valid CEPs
2
registered plants
24
filings across 6 regulators

Registered plants

Site FDA FEI
Tehsil Dera Bassi, India Not on file
SOLAN, India Not on file

What they file, and where

Molecule Regulators Docs
Cefepime SFDA (Saudi Arabia), US FDA 4
Ceftriaxone SFDA (Saudi Arabia), US FDA 4
Cefuroxime US FDA 4
Cefotaxime SFDA (Saudi Arabia), US FDA 3
Cefixime SFDA (Saudi Arabia), US FDA 2
Cefdinir US FDA 1
Cefpodoxime US FDA 1
Ceftazidime US FDA 1
Cefuroxime Axetil SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
ARCSA (EC) 5 None
ZAMRA (ZM) 5 None
EFDA (ET) 4 None
TMDA (TZ) 4 None
INVIMA (CO) 3 None
MINSA (CR) 3 None

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $104K 2
2025 $191.0M $43.8M 53
2024 $201.0M $76.3M 65
2023 $184.1M $86.0M 61

Export figures are customs aggregates. We do not publish the identity of any buyer. Revenue shown in US dollars, converted from the reported currency.

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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
Company filings
Revenue as reported