Suppliers / Chengdu Kanghong Biotech

Chengdu Kanghong Biotech

China 9 employees Updated 9 July 2026

Chengdu Kanghong Biotech is an API and finished-dose manufacturer based in China. It holds 3 valid CEPs across a filed portfolio of 3 molecules. Its filings concentrate with MEDSAFE (NZ), RAMA (GE) and NMPA (CN).

0
active US DMFs
3
valid CEPs
2
registered plants
90
filings across 7 regulators

Registered plants

Site FDA FEI
Pixian, United Arab Emirates Not on file
Chengdu, China Not on file

What they file, and where

Molecule Regulators Docs
Aprepitant EDQM 1
Bisoprolol EDQM 1
Rotigotine EDQM 1

Also appears on these molecule pages

Aprepitant API Bisoprolol API Oxacillin finished dose Rotigotine API

Filings and GMP by regulator

Regulator Filings GMP certificates
MEDSAFE (NZ) 48 None
RAMA (GE) 25 None
NMPA (CN) 11 None
MINSA (CR) 2 None
EEC_EAEU 2 None
DIGEMAPS (DO) 1 None

Questions about Chengdu Kanghong Biotech

Does Chengdu Kanghong Biotech hold a US DMF or a CEP?
Chengdu Kanghong Biotech holds 3 valid CEPs. 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.
Where does Chengdu Kanghong Biotech manufacture?
2 registered sites are on record, in United Arab Emirates and China (Pixian and Chengdu). Every site is listed on this page with the register it came from.
What does Chengdu Kanghong Biotech make?
3 molecules are on record against Chengdu Kanghong Biotech, including Aprepitant, Bisoprolol and Rotigotine. Each links through to that molecule's full manufacturer list.
Where does Chengdu Kanghong Biotech file?
Filings are on record with MEDSAFE (NZ), RAMA (GE), NMPA (CN), MINSA (CR) and 3 other regulators, 90 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.

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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