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PharmaCompass offers a list of Histamine Dihydrochloride 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 Histamine Dihydrochloride manufacturer or Histamine Dihydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Histamine Dihydrochloride manufacturer or Histamine Dihydrochloride supplier.
PharmaCompass also assists you with knowing the Histamine Dihydrochloride API Price utilized in the formulation of products. Histamine Dihydrochloride API Price is not always fixed or binding as the Histamine Dihydrochloride Price is obtained through a variety of data sources. The Histamine Dihydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ergotidine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ergotidine, including repackagers and relabelers. The FDA regulates Ergotidine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ergotidine 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 Ergotidine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ergotidine supplier is an individual or a company that provides Ergotidine active pharmaceutical ingredient (API) or Ergotidine finished formulations upon request. The Ergotidine suppliers may include Ergotidine API manufacturers, exporters, distributors and traders.
click here to find a list of Ergotidine 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 Ergotidine Drug Master File in Japan (Ergotidine JDMF) empowers Ergotidine 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 Ergotidine JDMF during the approval evaluation for pharmaceutical products. At the time of Ergotidine 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 Ergotidine suppliers with JDMF on PharmaCompass.
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