Suppliers / Chongqing Huapont Pharmaceutical

Chongqing Huapont Pharmaceutical

China Updated 9 July 2026

Chongqing Huapont Pharmaceutical is an API manufacturer based in China. It holds 17 active US drug master files across a filed portfolio of 15 molecules.

17
active US DMFs
0
valid CEPs
0
registered plants
0
filings across 0 regulators

What they file, and where

Molecule Regulators Docs
Bendamustine US FDA 2
Isotretinoin US FDA 2
Acitretin US FDA 1
Acrivastine US FDA 1
Dapsone US FDA 1
Dimethyl Fumarate US FDA 1
Fluticasone Propionate US FDA 1
Levocetirizine US FDA 1
Linezolid US FDA 1
Moxifloxacin US FDA 1
Show all 15 molecules on file
Naftifine US FDA 1
Paricalcitol US FDA 1
Roflumilast US FDA 1
Ruxolitinib US FDA 1
Tretinoin US FDA 1

Also appears on these molecule pages

Show 1 more molecule pages

Questions about Chongqing Huapont Pharmaceutical

Does Chongqing Huapont Pharmaceutical hold a US DMF or a CEP?
Chongqing Huapont Pharmaceutical holds 17 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 Chongqing Huapont Pharmaceutical make?
15 molecules are on record against Chongqing Huapont Pharmaceutical, including Bendamustine, Isotretinoin, Acitretin and Acrivastine. 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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Sources on this page

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