Suppliers / Flamingo Pharmaceuticals

Flamingo Pharmaceuticals

India 871 employees 2 duplicate records merged Updated 9 July 2026

Flamingo Pharmaceuticals is a finished-dose manufacturer based in India. It appears in 92 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with DAV (Vietnam), EFDA (ET) and DIGEMAPS (DO). Its GMP standing is certified by CDSCO (India), EMA and MHRA (UK). Customs aggregates show $59.9M of exports covering 1,907 molecules to 17 destinations in 2025.

0
active US DMFs
0
valid CEPs
4
registered plants
92
filings across 5 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
DIST. RAIGAD, India Not on file
Nanded, India Not on file
dc industrial estatepalejbharuch 392 220, India Not on file
Gidc, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 61 None
EFDA (ET) 11 None
DIGEMAPS (DO) 8 None
ZAMRA (ZM) 8 None
MINSA (CR) 4 None
CDSCO (India) None 2
EMA None 1
MHRA (UK) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $7.4M 10
2025 Not reported $59.9M 17
2024 Not reported $51.7M 25
2023 Not reported $47.9M 23

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 We do not publish the identity of any buyer.

Questions about Flamingo Pharmaceuticals

Does Flamingo Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Flamingo Pharmaceuticals. It does have 92 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Flamingo Pharmaceuticals manufacture?
4 registered sites are on record, in India (Dist. Raigad, Nanded and Dc Industrial Estatepalejbharuch 392 220 among others). Every site is listed on this page with the register it came from.
Which regulators recognise Flamingo Pharmaceuticals's GMP?
Current GMP certificates are on record from CDSCO (India), EMA and MHRA (UK). 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