Suppliers / Biodeal Pharmaceuticals

Biodeal Pharmaceuticals

India 334 employees 3 duplicate records merged Updated 9 July 2026

Biodeal Pharmaceuticals is a finished-dose manufacturer based in India. It appears in 40 regulatory filings across 7 regulators, without an active US DMF or CEP on file. Its filings concentrate with EFDA (ET), TMDA (TZ) and EEC_EAEU. Its GMP standing is certified by UZPHARM (UZ) and NAFDAC (NG). Customs aggregates show $2.8M of exports covering 303 molecules to 25 destinations in 2025.

0
active US DMFs
0
valid CEPs
1
registered plants
40
filings across 7 regulators

Registered plants

Site FDA FEI
t. Solan Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EFDA (ET) 14 None
TMDA (TZ) 9 None
EEC_EAEU 9 None
CDSCO (India) 3 None
ARCSA (EC) 2 None
UZPHARM (UZ) 2 2
NAFDAC (NG) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $413K 11
2025 Not reported $2.8M 25
2024 Not reported $2.0M 18
2023 Not reported $1.3M 13

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 We do not publish the identity of any buyer.

Questions about Biodeal Pharmaceuticals

Does Biodeal Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Biodeal Pharmaceuticals. It does have 40 filings with 7 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Biodeal Pharmaceuticals manufacture?
1 registered site is on record (T. Solan). Every site is listed on this page with the register it came from.
Which regulators recognise Biodeal Pharmaceuticals's GMP?
Current GMP certificates are on record from UZPHARM (UZ) and 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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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