Suppliers / Hubei Goto Biopharm

Hubei Goto Biopharm

China Updated 9 July 2026

Hubei Goto Biopharm is an API manufacturer based in China. It holds 2 active US drug master files across a filed portfolio of 2 molecules.

2
active US DMFs
0
valid CEPs
0
registered plants
0
filings across 0 regulators

What they file, and where

Molecule Regulators Docs
Prasterone US FDA 1
Testosterone US FDA 1

Also appears on these molecule pages

Prasterone API Testosterone contract manufacturing

Questions about Hubei Goto Biopharm

Does Hubei Goto Biopharm hold a US DMF or a CEP?
Hubei Goto Biopharm holds 2 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.
What does Hubei Goto Biopharm make?
2 molecules are on record against Hubei Goto Biopharm, including Prasterone and Testosterone. 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

Symbiotec Pharmalab shares 2 molecules Hubei Goto Biotechnology shares 2 molecules Dr Reddy's Laboratories shares 1 molecule Lupin shares 1 molecule Curia shares 1 molecule

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