Suppliers / Zeiss Pharmaceuticals

Zeiss Pharmaceuticals

India 2 duplicate records merged Updated 9 July 2026

Zeiss Pharmaceuticals is a finished-dose manufacturer based in India. It appears in 27 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with ARCSA (EC), NAFDAC (NG) and MINSA (CR). Its GMP standing is certified by FDA (GH). Customs aggregates show $870K of exports covering 59 molecules to 7 destinations in 2025.

0
active US DMFs
0
valid CEPs
0
registered plants
27
filings across 5 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
ARCSA (EC) 9 None
NAFDAC (NG) 8 None
MINSA (CR) 7 None
UZPHARM (UZ) 2 None
DAV (Vietnam) 1 None
FDA (GH) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $558K 4
2025 Not reported $870K 7
2024 Not reported $797K 7
2023 Not reported $1.0M 5

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 We do not publish the identity of any buyer.

Limited public record

Beyond the filing counts above, the public registers hold no plant, inspection or portfolio detail for this company as at 9 July 2026. We report that as a gap rather than inferring an answer.

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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