Suppliers / "Maneesh Pharmaceuticals"

"Maneesh Pharmaceuticals"

India 175 employees Updated 9 July 2026

"Maneesh Pharmaceuticals" is a finished-dose manufacturer based in India. It appears in 8 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with UZPHARM (UZ) and TMDA (TZ). Its GMP standing is certified by UZPHARM (UZ) and TMDA (TZ). Customs aggregates show $621K of exports covering 68 molecules to 12 destinations in 2025.

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

Registered plants

Site FDA FEI
Mumbai, India 3005074449

Filings and GMP by regulator

Regulator Filings GMP certificates
UZPHARM (UZ) 6 1
TMDA (TZ) 2 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $37K 2
2025 Not reported $621K 12
2024 Not reported $15.6M 44
2023 Not reported $14.7M 46

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 We do not publish the identity of any buyer.

Questions about "Maneesh Pharmaceuticals"

Does "Maneesh Pharmaceuticals" hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for "Maneesh Pharmaceuticals". It does have 8 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is "Maneesh Pharmaceuticals" FDA-registered?
One site operated by "Maneesh Pharmaceuticals" carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
Where does "Maneesh Pharmaceuticals" manufacture?
1 registered site is on record, in India (Mumbai). Every site is listed on this page with the register it came from.
Which regulators recognise "Maneesh Pharmaceuticals"'s GMP?
Current GMP certificates are on record from UZPHARM (UZ) and TMDA (TZ). 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