Fujian Genohope Biotech is a leading provider of high-potency peptide APIs, offering GMP quality and worldwide delivery.
01 1Fujian Genohope Biotech
02 2Allsino Pharmaceutical Co. Ltd
03 1Jiangsu Sinopep Allsino Biopharmaceutical
04 2Blank
01 4ORFORGLIPRON
02 1ORFORGLIPRON INTERMEDIATE III
03 1ORFORGLIPRON INTERMEDIATE IV
01 4China
02 2Blank
01 6Active
01 6Blank
Fujian Genohope Biotech is a leading provider of high-potency peptide APIs, offering GMP quality and worldwide delivery.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 42393
Submission : 2025-09-16
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 42503
Submission : 2025-09-04
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 42500
Submission : 2025-09-12
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 41815
Submission : 2025-04-27
Status : Active
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 43446
Submission : 2026-01-05
Status : Active
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 42012
Submission : 2025-05-26
Status : Active
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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A LY3502970 (Orforglipron) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LY3502970 (Orforglipron), including repackagers and relabelers. The FDA regulates LY3502970 (Orforglipron) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LY3502970 (Orforglipron) API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A LY3502970 (Orforglipron) supplier is an individual or a company that provides LY3502970 (Orforglipron) active pharmaceutical ingredient (API) or LY3502970 (Orforglipron) finished formulations upon request. The LY3502970 (Orforglipron) suppliers may include LY3502970 (Orforglipron) API manufacturers, exporters, distributors and traders.
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A LY3502970 (Orforglipron) DMF (Drug Master File) is a document detailing the whole manufacturing process of LY3502970 (Orforglipron) active pharmaceutical ingredient (API) in detail. Different forms of LY3502970 (Orforglipron) DMFs exist exist since differing nations have different regulations, such as LY3502970 (Orforglipron) USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A LY3502970 (Orforglipron) DMF submitted to regulatory agencies in the US is known as a USDMF. LY3502970 (Orforglipron) USDMF includes data on LY3502970 (Orforglipron)'s chemical properties, information on the facilities and procedures used, and details about packaging and storage. The LY3502970 (Orforglipron) USDMF is kept confidential to protect the manufacturer’s intellectual property.
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