Suppliers / Almelo

Almelo

India Updated 9 July 2026

Almelo is an API manufacturer based in India. It holds 4 active US drug master files across a filed portfolio of 4 molecules. Its filings concentrate with MINSA (CR) and CDSCO (India). Customs aggregates show $9.0M of exports covering 96 molecules to 26 destinations in 2025.

4
active US DMFs
0
valid CEPs
0
registered plants
3
filings across 2 regulators

What they file, and where

Molecule Regulators Docs
Sitagliptin SFDA (Saudi Arabia), US FDA 2
Pregabalin US FDA 1
Ranolazine US FDA 1
Sugammadex US FDA 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 2 None
CDSCO (India) 1 None

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $267K 6
2025 Not reported $9.0M 26
2024 Not reported $1.9M 29
2023 Not reported $4.1M 20

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 We do not publish the identity of any buyer.

Questions about Almelo

Does Almelo hold a US DMF or a CEP?
Almelo 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 Almelo make?
4 molecules are on record against Almelo, including Sitagliptin, Pregabalin, Ranolazine and Sugammadex. Each links through to that molecule's full manufacturer list.
Where does Almelo file?
Filings are on record with MINSA (CR) and CDSCO (India), 3 in total.

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