TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
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01 2TAPI Czech Industries s. r. o.
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01 1Ergotamine Tartrate
02 1Ergotamine tartrate "Teva"
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01 2Israel
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Registration Number : 307MF10007
Registrant's Address : Ostravska 305/29, Komarov, 747 70 Opava, Czech Republic
Initial Date of Registration : 2025-01-09
Latest Date of Registration : 2025-01-09
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Registration Number : 220MF10122
Registrant's Address : Ostravska 305/29, Komarov, 747 70 Opava, Czech Republic
Initial Date of Registration : 2008-04-28
Latest Date of Registration : 2008-04-28
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PharmaCompass offers a list of Ergotamine Tartrate 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 Ergotamine Tartrate manufacturer or Ergotamine Tartrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ergotamine Tartrate manufacturer or Ergotamine Tartrate supplier.
PharmaCompass also assists you with knowing the Ergotamine Tartrate API Price utilized in the formulation of products. Ergotamine Tartrate API Price is not always fixed or binding as the Ergotamine Tartrate Price is obtained through a variety of data sources. The Ergotamine Tartrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CAFERGOT-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAFERGOT-1, including repackagers and relabelers. The FDA regulates CAFERGOT-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAFERGOT-1 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 CAFERGOT-1 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CAFERGOT-1 supplier is an individual or a company that provides CAFERGOT-1 active pharmaceutical ingredient (API) or CAFERGOT-1 finished formulations upon request. The CAFERGOT-1 suppliers may include CAFERGOT-1 API manufacturers, exporters, distributors and traders.
click here to find a list of CAFERGOT-1 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 CAFERGOT-1 Drug Master File in Japan (CAFERGOT-1 JDMF) empowers CAFERGOT-1 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 CAFERGOT-1 JDMF during the approval evaluation for pharmaceutical products. At the time of CAFERGOT-1 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 CAFERGOT-1 suppliers with JDMF on PharmaCompass.
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