Suppliers / Sunways (India) Pvt.Ltd

Sunways (India) Pvt.Ltd

India 351 employees Updated 9 July 2026

Sunways (India) Pvt.Ltd is a finished-dose manufacturer based in India. It appears in 10 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with MINSA (CR), CDSCO (India) and UZPHARM (UZ). Its GMP standing is certified by CDSCO (India) and NAFDAC (NG). Customs aggregates show $957K of exports covering 335 molecules to 14 destinations in 2025.

0
active US DMFs
0
valid CEPs
2
registered plants
10
filings across 3 regulators

Registered plants

Site FDA FEI
ahm edabad, India Not on file
Ahmedabad, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 7 None
CDSCO (India) 2 2
UZPHARM (UZ) 1 None
NAFDAC (NG) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $127K 4
2025 Not reported $957K 14
2024 Not reported $1.2M 18
2023 Not reported $950K 18

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 We do not publish the identity of any buyer.

Questions about Sunways (India) Pvt.Ltd

Does Sunways (India) Pvt.Ltd hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Sunways (India) Pvt.Ltd. It does have 10 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Sunways (India) Pvt.Ltd manufacture?
2 registered sites are on record, in India and Nigeria (Ahm Edabad and Ahmedabad). Every site is listed on this page with the register it came from.
Which regulators recognise Sunways (India) Pvt.Ltd's GMP?
Current GMP certificates are on record from CDSCO (India) and NAFDAC (NG). 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