01 1Lonza Guangzhou Pharmaceutical Ltd
01 1Nicotinic acid amide
01 1Switzerland
Registration Number : 226MF10200
Registrant's Address : No. 1202, Building A1, No. 1, Qinghui Middle Road, Nansha District, Guangzhou
Initial Date of Registration : 2014-10-27
Latest Date of Registration : 2016-03-02
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PharmaCompass offers a list of Nicotinamide 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 Nicotinamide manufacturer or Nicotinamide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nicotinamide manufacturer or Nicotinamide supplier.
PharmaCompass also assists you with knowing the Nicotinamide API Price utilized in the formulation of products. Nicotinamide API Price is not always fixed or binding as the Nicotinamide Price is obtained through a variety of data sources. The Nicotinamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Niko-tamin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Niko-tamin, including repackagers and relabelers. The FDA regulates Niko-tamin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Niko-tamin 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 Niko-tamin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Niko-tamin supplier is an individual or a company that provides Niko-tamin active pharmaceutical ingredient (API) or Niko-tamin finished formulations upon request. The Niko-tamin suppliers may include Niko-tamin API manufacturers, exporters, distributors and traders.
click here to find a list of Niko-tamin 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 Niko-tamin Drug Master File in Japan (Niko-tamin JDMF) empowers Niko-tamin 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 Niko-tamin JDMF during the approval evaluation for pharmaceutical products. At the time of Niko-tamin 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 Niko-tamin suppliers with JDMF on PharmaCompass.
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