Does Hebei Veyong Pharmaceutical hold a US DMF or a CEP?
Hebei Veyong Pharmaceutical holds 1 valid CEP. 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 Hebei Veyong Pharmaceutical FDA-registered?
One site operated by Hebei Veyong Pharmaceutical 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 Hebei Veyong Pharmaceutical manufacture?
2 registered sites are on record, in China (China and Shijiazhuang). Every site is listed on this page with the register it came from.
What does Hebei Veyong Pharmaceutical make?
1 molecule is on record against Hebei Veyong Pharmaceutical, including Ivermectin. Each links through to that molecule's full manufacturer list.
Where does Hebei Veyong Pharmaceutical file?
Filings are on record with MINSA (CR), 1 in total.
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.