Is Yumen Qianhua Pharmaceutical Co., Ltd. FDA approved?

Yumen Qianhua Pharmaceutical Co., Ltd. holds 1 FDA-registered establishment in China. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.

Where are Yumen Qianhua Pharmaceutical Co., Ltd.'s drugs manufactured?

The FDA register lists Jiuquan City. Registered operations: analytical testing, active ingredient (API) manufacture, labelling, finished drug manufacture, packaging.

What drugs does Yumen Qianhua Pharmaceutical Co., Ltd. make?

3 products are listed under Yumen Qianhua Pharmaceutical Co., Ltd. in the openFDA NDC Directory, most often as powder. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Yumen Qianhua Pharmaceutical Co., Ltd.

Data as of 24 Sept 2026 · How to read this entry

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Registered sites: 1
Active NDC listings: 3
Live patents: 0
Countries: 1
Base: China

Authorisation

Registered operations

Analytical testing1Active ingredient (API) manufacture1Labelling1Finished drug manufacture1Packaging1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Yumen Qianhua Pharmaceutical Co., Ltd.	No. 8 Sanba Road, Old City Chemical Industry Park, Yumen City, Jiuquan City, Gansu Province 735299, China (CHN)	Analytical testing, Active ingredient (API) manufacture, Labelling, Finished drug manufacture, Packaging	3030638441722865195

Catalogue

Drug listings by form and route

3 active NDC listings: 3 bulk ingredient. By marketing category: BULK INGREDIENT 3.

Dosage form	NDCs
powder	3

Route	NDCs

Labeller name on the listing	NDCs
yumen qianhua pharmaceutical co., ltd.	3

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	Cromolyn Sodium	powder	84317-101BULK INGREDIENT
-	Dyclonine Hydrochloride	powder	84317-103BULK INGREDIENT
-	Methimazol	powder	84317-102BULK INGREDIENT

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Enquiry

Common questions

Is Yumen Qianhua Pharmaceutical Co., Ltd. FDA approved?: Yumen Qianhua Pharmaceutical Co., Ltd. holds 1 FDA-registered establishment in China. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
Where are Yumen Qianhua Pharmaceutical Co., Ltd.'s drugs manufactured?: The FDA register lists Jiuquan City. Registered operations: analytical testing, active ingredient (API) manufacture, labelling, finished drug manufacture, packaging.
What drugs does Yumen Qianhua Pharmaceutical Co., Ltd. make?: 3 products are listed under Yumen Qianhua Pharmaceutical Co., Ltd. in the openFDA NDC Directory, most often as powder. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.