Suppliers / Farbe Firma Pvt.Ltd

Farbe Firma Pvt.Ltd

India 27 employees 4 duplicate records merged Updated 9 July 2026

Farbe Firma Pvt.Ltd is a finished-dose manufacturer based in India. It appears in 34 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with NAFDAC (NG), UZPHARM (UZ) and ARCSA (EC). Its GMP standing is certified by NAFDAC (NG), CDSCO (India) and FDA (GH), among 5 authorities. Customs aggregates show $1.6M of exports covering 122 molecules to 20 destinations in 2025.

0
active US DMFs
0
valid CEPs
3
registered plants
34
filings across 5 regulators

Registered plants

Site FDA FEI
Ankleshwar, India Not on file
ankleshwar 393 002bharuch, India Not on file
Bharuch, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
NAFDAC (NG) 19 2
UZPHARM (UZ) 6 1
ARCSA (EC) 5 None
MINSA (CR) 3 None
EFDA (ET) 1 None
CDSCO (India) None 2
FDA (GH) None 1
ZAMRA (ZM) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $15K 2
2025 Not reported $1.6M 20
2024 Not reported $1.7M 23
2023 Not reported $830K 14

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 We do not publish the identity of any buyer.

Questions about Farbe Firma Pvt.Ltd

Does Farbe Firma Pvt.Ltd hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Farbe Firma Pvt.Ltd. It does have 34 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Farbe Firma Pvt.Ltd manufacture?
3 registered sites are on record, in India and Nigeria (Ankleshwar, Ankleshwar 393 002bharuch and Bharuch). Every site is listed on this page with the register it came from.
Which regulators recognise Farbe Firma Pvt.Ltd's GMP?
Current GMP certificates are on record from NAFDAC (NG), CDSCO (India), FDA (GH), UZPHARM (UZ) and ZAMRA (ZM). 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