Suppliers / Acebright India Pharma

Acebright India Pharma

India Updated 9 July 2026

Acebright India Pharma is an API manufacturer based in India. It holds 4 active US drug master files across a filed portfolio of 7 molecules. Customs aggregates show $347 of exports covering 82 molecules to 4 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
Imatinib US FDA 2
Dabigatran US FDA 1
Dasatinib SFDA (Saudi Arabia) 1
Erlotinib SFDA (Saudi Arabia) 1
Imatinib Mesilate SFDA (Saudi Arabia) 1
Lopinavir US FDA 1
Tenofovir Disoproxil SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Scale

Year Revenue Exports Destinations
2025 Not reported $347 4
2024 Not reported $22 1
2023 Not reported $1.2M 12
2022 Not reported $12.1M 18

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 We do not publish the identity of any buyer.

Questions about Acebright India Pharma

Does Acebright India Pharma hold a US DMF or a CEP?
Acebright India Pharma 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 Acebright India Pharma make?
7 molecules are on record against Acebright India Pharma, including Imatinib, Dabigatran, Dasatinib and Erlotinib. 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