Suppliers / "Ultra Laboratories

"Ultra Laboratories

India Updated 9 July 2026

"Ultra Laboratories is a finished-dose manufacturer based in India. It appears in 77 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with UZPHARM (UZ), ARCSA (EC) and MINSA (CR). Its GMP standing is certified by CDSCO (India) and UZPHARM (UZ). Customs aggregates show $2.9M of exports covering 138 molecules to 5 destinations in 2025.

0
active US DMFs
0
valid CEPs
2
registered plants
77
filings across 3 regulators

Registered plants

Site FDA FEI
Hassan, India Not on file
hassan 573 201, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
UZPHARM (UZ) 72 1
ARCSA (EC) 3 None
MINSA (CR) 2 None
CDSCO (India) None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $267K 2
2025 Not reported $2.9M 5
2024 Not reported $5.8M 7
2023 Not reported $3.5M 4

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 We do not publish the identity of any buyer.

Questions about "Ultra Laboratories

Does "Ultra Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for "Ultra Laboratories. It does have 77 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does "Ultra Laboratories manufacture?
2 registered sites are on record, in India (Hassan and Hassan 573 201). Every site is listed on this page with the register it came from.
Which regulators recognise "Ultra Laboratories's GMP?
Current GMP certificates are on record from CDSCO (India) and UZPHARM (UZ). 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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Comparable suppliers

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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