Is Yung Shin Pharm. Ind. Co., Ltd. FDA approved?

Yung Shin Pharm. Ind. Co., Ltd. holds 1 FDA-registered establishment in Taiwan. 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 Yung Shin Pharm. Ind. Co., Ltd.'s drugs manufactured?

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

What drugs does Yung Shin Pharm. Ind. Co., Ltd. make?

5 products are listed under Yung Shin Pharm. Ind. 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.

Yung Shin Pharm. Ind. Co., Ltd.

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

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Registered sites: 1
Active NDC listings: 5
Live patents: 0
Countries: 1
Base: Taiwan

Authorisation

Registered operations

Analytical testing1Active ingredient (API) manufacture1Labelling1Finished drug manufacture1Packaging1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
YUNG SHIN PHARM. IND. CO., LTD. (TAICHUNG YOUTH FACTORY)Registrant: Yung Shin Pharm. Ind. Co., Ltd.	No. 1191, Sec. 1, Zhongshan Rd., Dajia Dist., Taichung City, 437003, Taiwan (TWN)	Analytical testing, Active ingredient (API) manufacture, Labelling, Finished drug manufacture, Packaging	3002808536656108149

Catalogue

Drug listings by form and route

5 active NDC listings: 5 bulk ingredient. By marketing category: BULK INGREDIENT 5.

Dosage form	NDCs
powder	5

Route	NDCs

Labeller name on the listing	NDCs
yung shin pharm. ind. co., ltd.	5

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	Cabazitaxel	powder	63126-909BULK INGREDIENT
-	Cinacalcet Hydrochloride	powder	63126-910BULK INGREDIENT
-	Famotidine	powder	63126-907BULK INGREDIENT
-	Micafungin Sodium	powder	63126-908BULK INGREDIENT
-	Voriconazole	powder	63126-911BULK INGREDIENT

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Enquiry

Common questions

Is Yung Shin Pharm. Ind. Co., Ltd. FDA approved?: Yung Shin Pharm. Ind. Co., Ltd. holds 1 FDA-registered establishment in Taiwan. 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 Yung Shin Pharm. Ind. Co., Ltd.'s drugs manufactured?: The FDA register lists Taichung City. Registered operations: analytical testing, active ingredient (API) manufacture, labelling, finished drug manufacture, packaging.
What drugs does Yung Shin Pharm. Ind. Co., Ltd. make?: 5 products are listed under Yung Shin Pharm. Ind. 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.