TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 2TAPI Czech Industries s. r. o.
02 1Olon S. p. A.
01 2Nicergoline
02 1Nicergoline "Teva"
01 1Israel
02 1Italy
03 1Blank
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Registration Number : 220MF10070
Registrant's Address : Ostravska 305/29, Komarov, 747 70 Opava, Czech Republic
Initial Date of Registration : 2008-02-25
Latest Date of Registration : 2008-02-25
Registration Number : 218MF10446
Registrant's Address : Strada Rivoltana Km 6/7 20053 Rodano Milano Italy
Initial Date of Registration : 2006-04-27
Latest Date of Registration : 2007-12-19
Registration Number : 306MF10154
Registrant's Address : Ostravska 305/29, Komarov, 747 70 Opava, Czech Republic
Initial Date of Registration : 2024-12-04
Latest Date of Registration : 2024-12-04
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A Nicergoline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nicergoline, including repackagers and relabelers. The FDA regulates Nicergoline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nicergoline 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 Nicergoline manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nicergoline supplier is an individual or a company that provides Nicergoline active pharmaceutical ingredient (API) or Nicergoline finished formulations upon request. The Nicergoline suppliers may include Nicergoline API manufacturers, exporters, distributors and traders.
click here to find a list of Nicergoline 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 Nicergoline Drug Master File in Japan (Nicergoline JDMF) empowers Nicergoline 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 Nicergoline JDMF during the approval evaluation for pharmaceutical products. At the time of Nicergoline 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 Nicergoline suppliers with JDMF on PharmaCompass.
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