Suppliers / Erythro Pharma

Erythro Pharma

India Updated 9 July 2026

Erythro Pharma is an API manufacturer based in India. It holds 4 active US drug master files across a filed portfolio of 3 molecules. Customs aggregates show $326K of exports covering 11 molecules to 8 destinations in 2025.

4
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026.

Registered plants

Site FDA FEI
Sangareddy District, India 3003945855

What they file, and where

Molecule Regulators Docs
Prucalopride US FDA 2
Gepirone US FDA 1
Tafamidis US FDA 1

Also appears on these molecule pages

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $53K 1
2025 Not reported $326K 8
2024 Not reported $173K 3
2023 Not reported $573K 3

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 We do not publish the identity of any buyer.

Questions about Erythro Pharma

Does Erythro Pharma hold a US DMF or a CEP?
Erythro 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.
Is Erythro Pharma FDA-registered?
One site operated by Erythro Pharma carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
Where does Erythro Pharma manufacture?
1 registered site is on record, in India (Sangareddy District). Every site is listed on this page with the register it came from.
What does Erythro Pharma make?
3 molecules are on record against Erythro Pharma, including Prucalopride, Gepirone and Tafamidis. 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