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Teva API has over 350 products in its portfolio and is the leading international supplier of APIs. 
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01 Teva Czech Industries s. r. o. (1)
02 YS Life Science Co. , Ltd. (1)
01 Cabergoline (2)
01 Israel (1)
02 South Korea (1)
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PharmaCompass offers a list of Cabergoline 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 Cabergoline manufacturer or Cabergoline supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cabergoline manufacturer or Cabergoline supplier.
PharmaCompass also assists you with knowing the Cabergoline API Price utilized in the formulation of products. Cabergoline API Price is not always fixed or binding as the Cabergoline Price is obtained through a variety of data sources. The Cabergoline Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cabergoline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cabergoline, including repackagers and relabelers. The FDA regulates Cabergoline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cabergoline 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 Cabergoline manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cabergoline supplier is an individual or a company that provides Cabergoline active pharmaceutical ingredient (API) or Cabergoline finished formulations upon request. The Cabergoline suppliers may include Cabergoline API manufacturers, exporters, distributors and traders.
click here to find a list of Cabergoline suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Cabergoline Drug Master File in Japan (Cabergoline JDMF) empowers Cabergoline API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Cabergoline JDMF during the approval evaluation for pharmaceutical products. At the time of Cabergoline JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Cabergoline suppliers with JDMF on PharmaCompass.
We have 2 companies offering Cabergoline
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