Trusted Partner for Innovative, Sustainable, and High-Quality API Development and Production.
01 1Alven Laboratories sro
02 1PharmaZell GmbH
03 1(주)애거슨바이오
04 1Janssen Pharmaceutica NV
05 1Shilpa Pharma Lifesciences Limited
06 1Symed Labs Ltd (Unit-Ⅰ)
Trusted Partner for Innovative, Sustainable, and High-Quality API Development and Production.
Registrant Name : Hwail Pharmaceutical Co., Ltd.
Registration Date : 2019-11-13
Registration Number : Su331-18-ND
Manufacturer Name : Alven Laboratories sro
Manufacturer Address : Holická 1173/49a, Hodolany, 779 00 Olomouc, Czech Republic
Axplora is your partner of choice for complex APIs.
Registrant Name : Menarini Korea Co., Ltd.
Registration Date : 2025-01-17
Registration Number : 11-3-ND
Manufacturer Name : PharmaZell GmbH
Manufacturer Address : Rosenheimer Straße 43 83064 Raubling Germany
90
PharmaCompass offers a list of Prucalopride Succinate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Prucalopride Succinate manufacturer or Prucalopride Succinate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Prucalopride Succinate manufacturer or Prucalopride Succinate supplier.
PharmaCompass also assists you with knowing the Prucalopride Succinate API Price utilized in the formulation of products. Prucalopride Succinate API Price is not always fixed or binding as the Prucalopride Succinate Price is obtained through a variety of data sources. The Prucalopride Succinate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 179474-85-2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 179474-85-2, including repackagers and relabelers. The FDA regulates 179474-85-2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 179474-85-2 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of 179474-85-2 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 179474-85-2 supplier is an individual or a company that provides 179474-85-2 active pharmaceutical ingredient (API) or 179474-85-2 finished formulations upon request. The 179474-85-2 suppliers may include 179474-85-2 API manufacturers, exporters, distributors and traders.
click here to find a list of 179474-85-2 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a 179474-85-2 Drug Master File in Korea (179474-85-2 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 179474-85-2. The MFDS reviews the 179474-85-2 KDMF as part of the drug registration process and uses the information provided in the 179474-85-2 KDMF to evaluate the safety and efficacy of the drug.
After submitting a 179474-85-2 KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their 179474-85-2 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of 179474-85-2 suppliers with KDMF on PharmaCompass.
We have 5 companies offering 179474-85-2
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