Suppliers / Smaart Pharmaceutticals

Smaart Pharmaceutticals

India 32 employees Updated 9 July 2026

Smaart Pharmaceutticals 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 $677K of exports covering 75 molecules to 20 destinations in 2025.

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

What they file, and where

Molecule Regulators Docs
Chlorhexidine US FDA 1
Nebivolol US FDA 1

Also appears on these molecule pages

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $238K 11
2025 Not reported $677K 20
2024 Not reported $524K 18
2023 Not reported $811K 21

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 We do not publish the identity of any buyer.

Questions about Smaart Pharmaceutticals

Does Smaart Pharmaceutticals hold a US DMF or a CEP?
Smaart Pharmaceutticals 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.
What does Smaart Pharmaceutticals make?
2 molecules are on record against Smaart Pharmaceutticals, including Chlorhexidine and Nebivolol. 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