Suppliers / Appasamy Ocular Devices Pvt.Ltd

Appasamy Ocular Devices Pvt.Ltd

India 2 duplicate records merged Updated 9 July 2026

Appasamy Ocular Devices Pvt.Ltd is a finished-dose manufacturer based in India. It appears in 19 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with EFDA (ET), ZAMRA (ZM) and UZPHARM (UZ). Its GMP standing is certified by CDSCO (India). Customs aggregates show $60K of exports covering 20 molecules to 2 destinations in 2023.

0
active US DMFs
0
valid CEPs
2
registered plants
19
filings across 5 regulators

Registered plants

Site FDA FEI
Vadamangalam, India Not on file
puducherry 605102, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EFDA (ET) 10 None
ZAMRA (ZM) 5 None
UZPHARM (UZ) 2 None
ARCSA (EC) 1 None
CDSCO (India) 1 2

Scale

Year Revenue Exports Destinations
2023 Not reported $60K 2
2022 Not reported $37K 2

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 We do not publish the identity of any buyer.

Questions about Appasamy Ocular Devices Pvt.Ltd

Does Appasamy Ocular Devices Pvt.Ltd hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Appasamy Ocular Devices Pvt.Ltd. It does have 19 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Appasamy Ocular Devices Pvt.Ltd manufacture?
2 registered sites are on record, in India (Vadamangalam and Puducherry 605102). Every site is listed on this page with the register it came from.
Which regulators recognise Appasamy Ocular Devices Pvt.Ltd'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. Appasamy Ocular Devices Pvt.Ltd 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
Customs aggregates
Export values, molecule and destination counts