Is Zhejiang Peptites Biotech Co Ltd FDA approved?

Zhejiang Peptites Biotech 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 Zhejiang Peptites Biotech Co Ltd's drugs manufactured?

The FDA register lists Shaoxing City. Registered operations: analytical testing, active ingredient (API) manufacture.

What drugs does Zhejiang Peptites Biotech Co Ltd make?

4 products are listed under Zhejiang Peptites Biotech 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.

Zhejiang Peptites Biotech Co Ltd

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

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Registered sites: 1
Active NDC listings: 4
Labeller names: 2
Live patents: 0
Countries: 1
Base: China

Authorisation

Registered operations

Analytical testing1Active ingredient (API) manufacture1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Zhejiang Peptites Biotech Co., LtdRegistrant: Zhejiang Peptites Biotech Co Ltd	No.8,Hengyizhi Road, Sanjie Town, Shengzhou City, Shaoxing City, Zhejiang 312452, China (CHN)	Analytical testing, Active ingredient (API) manufacture	3015685285560465455

Catalogue

Drug listings by form and route

4 active NDC listings: 4 bulk ingredient. By marketing category: BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING 4.

Dosage form	NDCs
powder	4

Route	NDCs

Labeller name on the listing	NDCs
zhejiang peptites biotech co., ltd.	3
zhejiang peptites biotech co., ltd	1

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	Leuprolide Acetate	powder	73569-076BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-	Liraglutide	powder	73569-051BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-	Semaglutide	powder	73569-035BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-	Tirzepatide	powder	73569-050BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

Compare

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Shandong New Time Pharmaceutical Co., Ltd.1 site · 29 NDC
Anqiu Lu'an Pharmaceutical Co., Ltd.1 site · 27 NDC
Hainan Poly Pharm. Co., Ltd.1 site · 27 NDC
Qingdao Qinzeyuan Biotechnology Co Ltd1 site · 27 NDC
Shenzhen Alvantis Pharma Co., Ltd.1 site · 27 NDC
El-Peptido (Shanghai) Biopharmaceutical Co., Ltd1 site · 25 NDC

Enquiry

Common questions

Is Zhejiang Peptites Biotech Co Ltd FDA approved?: Zhejiang Peptites Biotech 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 Zhejiang Peptites Biotech Co Ltd's drugs manufactured?: The FDA register lists Shaoxing City. Registered operations: analytical testing, active ingredient (API) manufacture.
What drugs does Zhejiang Peptites Biotech Co Ltd make?: 4 products are listed under Zhejiang Peptites Biotech 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.