Suppliers / Sai Sreyas Pharmaceutical

Sai Sreyas Pharmaceutical

India Updated 9 July 2026

Sai Sreyas Pharmaceutical is an API manufacturer based in India. It holds 11 active US drug master files across a filed portfolio of 6 molecules. Customs aggregates show $205K of exports covering 22 molecules to 7 destinations in 2025.

11
active US DMFs
0
valid CEPs
0
registered plants
0
filings across 0 regulators

What they file, and where

Molecule Regulators Docs
Rivaroxaban US FDA 3
Empagliflozin US FDA 2
Olanzapine US FDA 2
Resmetirom US FDA 2
Alectinib US FDA 1
Sitagliptin US FDA 1

Also appears on these molecule pages

Scale

Year Revenue Exports Destinations
2025 Not reported $205K 7
2024 Not reported $35K 4
2023 Not reported $227 1
2022 Not reported $712 1

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 We do not publish the identity of any buyer.

Questions about Sai Sreyas Pharmaceutical

Does Sai Sreyas Pharmaceutical hold a US DMF or a CEP?
Sai Sreyas Pharmaceutical holds 11 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 Sai Sreyas Pharmaceutical make?
6 molecules are on record against Sai Sreyas Pharmaceutical, including Rivaroxaban, Empagliflozin, Olanzapine and Resmetirom. 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