Suppliers / Dhanuka Laboratories

Dhanuka Laboratories

India Updated 9 July 2026

Dhanuka Laboratories is an API and finished-dose manufacturer based in India. It appears in 2 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with CDSCO (India) and MINSA (CR). Customs aggregates show $28.6M of exports covering 263 molecules to 16 destinations in 2025.

0
active US DMFs
0
valid CEPs
1
registered plants
2
filings across 2 regulators

Registered plants

Site FDA FEI
Gurgaon, India Not on file

What they file, and where

Molecule Regulators Docs
Cefixime SFDA (Saudi Arabia) 1
Cefpodoxim Proxetil SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Cefixime API Elagolix finished dose

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) 1 None
MINSA (CR) 1 None

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $6.2M 9
2025 Not reported $28.6M 16
2024 Not reported $29.8M 17
2023 Not reported $22.7M 14

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 We do not publish the identity of any buyer.

Questions about Dhanuka Laboratories

Does Dhanuka Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Dhanuka Laboratories. It does have 2 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Dhanuka Laboratories manufacture?
1 registered site is on record, in India (Gurgaon). Every site is listed on this page with the register it came from.
What does Dhanuka Laboratories make?
2 molecules are on record against Dhanuka Laboratories, including Cefixime and Cefpodoxim Proxetil. Each links through to that molecule's full manufacturer list.
Where does Dhanuka Laboratories file?
Filings are on record with CDSCO (India) and MINSA (CR), 2 in total.

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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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
Customs aggregates
Export values, molecule and destination counts