Suppliers / Surya Remedies

Surya Remedies

India Updated 9 July 2026

Surya Remedies is an API manufacturer based in India. It holds one valid CEP. Its GMP standing is certified by CDSCO (India). Customs aggregates show $952K of exports covering 50 molecules to 10 destinations in 2025.

0
active US DMFs
1
valid CEPs
3
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Ankleshwar, India Not on file
ankleshwar 393 002bharuch, India Not on file
Ankleshwar, India Not on file

What they file, and where

Molecule Regulators Docs
Bromhexine EDQM 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $87K 4
2025 Not reported $952K 10
2024 Not reported $1.4M 14
2023 Not reported $616K 12

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 We do not publish the identity of any buyer.

Questions about Surya Remedies

Does Surya Remedies hold a US DMF or a CEP?
Surya Remedies holds 1 valid CEP. 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.
Where does Surya Remedies manufacture?
3 registered sites are on record, in India (Ankleshwar and Ankleshwar 393 002bharuch among others). Every site is listed on this page with the register it came from.
What does Surya Remedies make?
1 molecule is on record against Surya Remedies, including Bromhexine. Each links through to that molecule's full manufacturer list.
Which regulators recognise Surya Remedies's GMP?
Current GMP certificates are on record from CDSCO (India). GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

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
EudraGMDP and national regulators
GMP certificates
Customs aggregates
Export values, molecule and destination counts