Suppliers / Labdhi Pharmaceuticals

Labdhi Pharmaceuticals

India Updated 9 July 2026

Labdhi Pharmaceuticals is a finished-dose manufacturer based in India. It appears in 23 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by CDSCO (India). Customs aggregates show $1.9M of exports covering 230 molecules to 8 destinations in 2025.

0
active US DMFs
0
valid CEPs
4
registered plants
23
filings across 1 regulators

Registered plants

Site FDA FEI
ahmedabad 382 481, India Not on file
himatnagar 383 001sabarkantha, India Not on file
Gidc, India Not on file
tal kalolchhatralgand hinagar, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 23 None
CDSCO (India) None 4

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $234K 6
2025 Not reported $1.9M 8
2024 Not reported $1.3M 10
2023 Not reported $737K 17

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 We do not publish the identity of any buyer.

Questions about Labdhi Pharmaceuticals

Does Labdhi Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Labdhi Pharmaceuticals. It does have 23 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Labdhi Pharmaceuticals manufacture?
4 registered sites are on record, in India (Ahmedabad 382 481, Himatnagar 383 001sabarkantha and Gidc among others). Every site is listed on this page with the register it came from.
Which regulators recognise Labdhi Pharmaceuticals'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.

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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