Suppliers / Sms Lifesciences India

Sms Lifesciences India

India 121 employees Updated 9 July 2026

The public registers hold a second record for Sms Lifesciences India. The fuller profile, with 41 active US DMFs and 22 valid CEPs, is at SMS Pharmaceuticals. Figures on this page cover only this record.

Sms Lifesciences India is an API manufacturer based in India. It holds 4 active US drug master files across a filed portfolio of 4 molecules. Customs aggregates show $12.7M of exports covering 249 molecules to 39 destinations in 2025.

4
active US DMFs
0
valid CEPs
0
registered plants
0
filings across 0 regulators

What they file, and where

Molecule Regulators Docs
Cimetidine US FDA 1
Famotidine US FDA 1
Furosemide US FDA 1
Minoxidil US FDA 1

Also appears on these molecule pages

Scale

Year Revenue Exports Destinations
2025 Not reported $12.7M 39
2024 Not reported $13.9M 39
2023 Not reported $15.7M 37
2022 Not reported $14.4M 39

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 We do not publish the identity of any buyer.

Questions about Sms Lifesciences India

Does Sms Lifesciences India hold a US DMF or a CEP?
Sms Lifesciences India holds 4 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 Sms Lifesciences India make?
4 molecules are on record against Sms Lifesciences India, including Cimetidine, Famotidine, Furosemide and Minoxidil. 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.

Comparing suppliers?

Choose your molecules and target markets. Sms Lifesciences India comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Comparable suppliers

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