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

Bupivacaine API Epinephrine API Norepinephrine API Phenylephrine API

Questions about Zhejiang Boxiao Biopharmaceutical

Does Zhejiang Boxiao Biopharmaceutical hold a US DMF or a CEP?
Zhejiang Boxiao Biopharmaceutical holds 6 active US drug master files. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Is Zhejiang Boxiao Biopharmaceutical FDA-registered?
One site operated by Zhejiang Boxiao Biopharmaceutical carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
Where does Zhejiang Boxiao Biopharmaceutical manufacture?
1 registered site is on record, in China (China). Every site is listed on this page with the register it came from.
What does Zhejiang Boxiao Biopharmaceutical make?
5 molecules are on record against Zhejiang Boxiao Biopharmaceutical, including Epinephrine, Bupivacaine, Methylergometrine and Norepinephrine. Each links through to that molecule's full manufacturer list.

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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Comparable suppliers

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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