Suppliers / Sunways Rohto Pharmaceutical Private Limited 803,804,805

Sunways Rohto Pharmaceutical Private Limited 803,804,805

India Updated 9 July 2026

Sunways Rohto Pharmaceutical Private Limited 803,804,805 is a finished-dose manufacturer based in India. It appears in 16 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by CDSCO (India).

0
active US DMFs
0
valid CEPs
4
registered plants
16
filings across 1 regulators

Registered plants

Site FDA FEI
dholka ahmedabad, India Not on file
G.I.D.C., India Not on file
ahmedabad, India Not on file
Ahmedabad, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
NAFDAC (NG) 16 None
CDSCO (India) None 4

Questions about Sunways Rohto Pharmaceutical Private Limited 803,804,805

Does Sunways Rohto Pharmaceutical Private Limited 803,804,805 hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Sunways Rohto Pharmaceutical Private Limited 803,804,805. It does have 16 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Sunways Rohto Pharmaceutical Private Limited 803,804,805 manufacture?
4 registered sites are on record, in India (Dholka Ahmedabad, G.i.d.c. and Ahmedabad among others). Every site is listed on this page with the register it came from.
Which regulators recognise Sunways Rohto Pharmaceutical Private Limited 803,804,805'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.

Comparing suppliers?

Choose your molecules and target markets. Sunways Rohto Pharmaceutical Private Limited 803,804,805 comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Comparable suppliers

Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates