
Reset all filters
01 1Glaxo Wellcome Manufacturing Pte Ltd
02 2HIKAL Ltd.
Reset all filters
01 1Samil Pharmaceutical Co., Ltd.
02 1Seongi Bio Co., Ltd.
03 1Sungjin Exim Co., Ltd.
Reset all filters
01 3Ondansetron
Reset all filters
01 2India
02 1United Kingdom
Registrant Name : Samil Pharmaceutical Co., Ltd.
Registration Date : 2010-12-30
Registration Number : 20101230-47-B-303-15
Manufacturer Name : Glaxo Wellcome Manufacturing...
Manufacturer Address : 1 Pioneer Sector 1 Singapore 628413
Registrant Name : Sungjin Exim Co., Ltd.
Registration Date : 2013-05-10
Registration Number : 20130510-47-B-349-18
Manufacturer Name : HIKAL Ltd.
Manufacturer Address : 82/A, KIADB Industrial Area, Jigani, Anekal Taluk, Bangalore-562105, Karnataka, India
Registrant Name : Seongi Bio Co., Ltd.
Registration Date : 2020-06-19
Registration Number : 20130510-47-B-349-18(2)
Manufacturer Name : HIKAL Ltd.
Manufacturer Address : 82/A, KIADB Industrial Area, Jigani, Anekal Taluk, Bangalore-562105, Karnataka, India
87
PharmaCompass offers a list of Ondansetron 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 Ondansetron manufacturer or Ondansetron supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ondansetron manufacturer or Ondansetron supplier.
PharmaCompass also assists you with knowing the Ondansetron API Price utilized in the formulation of products. Ondansetron API Price is not always fixed or binding as the Ondansetron Price is obtained through a variety of data sources. The Ondansetron Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AB2000413 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AB2000413, including repackagers and relabelers. The FDA regulates AB2000413 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AB2000413 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 AB2000413 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AB2000413 supplier is an individual or a company that provides AB2000413 active pharmaceutical ingredient (API) or AB2000413 finished formulations upon request. The AB2000413 suppliers may include AB2000413 API manufacturers, exporters, distributors and traders.
click here to find a list of AB2000413 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 AB2000413 Drug Master File in Korea (AB2000413 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of AB2000413. The MFDS reviews the AB2000413 KDMF as part of the drug registration process and uses the information provided in the AB2000413 KDMF to evaluate the safety and efficacy of the drug.
After submitting a AB2000413 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 AB2000413 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of AB2000413 suppliers with KDMF on PharmaCompass.