Suppliers / Lesanto Laboratories

Lesanto Laboratories

India 33 employees Updated 9 July 2026

Lesanto Laboratories is a finished-dose manufacturer based in India. It appears in 90 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with NAFDAC (NG), FDA (GH) and MINSA (CR). Its GMP standing is certified by NAFDAC (NG). Customs aggregates show $41K of exports covering 5 molecules to 2 destinations in 2025.

0
active US DMFs
0
valid CEPs
1
registered plants
90
filings across 3 regulators

Registered plants

Site FDA FEI
Thane, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
NAFDAC (NG) 80 2
FDA (GH) 5 None
MINSA (CR) 5 None

Scale

Year Revenue Exports Destinations
2025 Not reported $41K 2
2024 Not reported $31K 2
2023 Not reported $219K 4
2022 Not reported $9K 1

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 We do not publish the identity of any buyer.

Questions about Lesanto Laboratories

Does Lesanto Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Lesanto Laboratories. It does have 90 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Lesanto Laboratories manufacture?
1 registered site is on record, in Nigeria (Thane). Every site is listed on this page with the register it came from.
Which regulators recognise Lesanto Laboratories's GMP?
Current GMP certificates are on record from NAFDAC (NG). 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

Abbott Healthcare also in India Accent Pharmaceuticals Diagnostics also in India Accure Labs Pvt.Ltd also in India ACME Formulation also in India Acme Generics also in India

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