Does Hangzhou Hotide Biotech Co.,Ltd hold a US DMF or a CEP?
Hangzhou Hotide Biotech Co.,Ltd 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.
Is Hangzhou Hotide Biotech Co.,Ltd FDA-registered?
One site operated by Hangzhou Hotide Biotech Co.,Ltd 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 Hangzhou Hotide Biotech Co.,Ltd 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 Hangzhou Hotide Biotech Co.,Ltd make?
1 molecule is on record against Hangzhou Hotide Biotech Co.,Ltd, including Tirzepatide. 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.