Suppliers / Shodhana Laboratories

Shodhana Laboratories

India 128 employees Updated 9 July 2026

Shodhana Laboratories is a contract manufacturer based in India. It holds 8 active US drug master files across a filed portfolio of 5 molecules. Its GMP standing is certified by MFDS (Korea). Customs aggregates show $9.6M of exports covering 214 molecules to 42 destinations in 2025.

8
active US DMFs
0
valid CEPs
2
registered plants 2 with an FDA FEI number
1
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
2 of 2 confirmed
Sources: FDA Establishment Registration, read 4 May 2026.

Registered plants

Site FDA FEI
Hyderabad, India 3010836438
Visakhapatnam, India 3029445647

What they file, and where

Molecule Regulators Docs
Carvedilol SFDA (Saudi Arabia), US FDA 3
Escitalopram SFDA (Saudi Arabia), US FDA 3
Duloxetine US FDA 2
Rivastigmine US FDA 2
Ondansetron SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 1 None
MFDS (Korea) None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $1.5M 19
2025 Not reported $9.6M 42
2024 Not reported $9.5M 37
2023 Not reported $6.9M 34

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 We do not publish the identity of any buyer.

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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