Suppliers / Zhejiang Boxiao Biopharmaceutical

Zhejiang Boxiao Biopharmaceutical

China Updated 9 July 2026

Zhejiang Boxiao Biopharmaceutical is an API manufacturer based in China. It holds 6 active US drug master files across a filed portfolio of 5 molecules.

6
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
0
filings across 0 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
China, China 3039398301

What they file, and where

Molecule Regulators Docs
Epinephrine US FDA 2
Bupivacaine US FDA 1
Methylergometrine US FDA 1
Norepinephrine US FDA 1
Phenylephrine US FDA 1

Also appears on these molecule pages

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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability