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 Niacinamide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Niacinamide manufacturer or Niacinamide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Niacinamide manufacturer or Niacinamide supplier.
A Nicotinamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nicotinamide, including repackagers and relabelers. The FDA regulates Nicotinamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nicotinamide 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 Nicotinamide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Nicotinamide supplier is an individual or a company that provides Nicotinamide active pharmaceutical ingredient (API) or Nicotinamide finished formulations upon request. The Nicotinamide suppliers may include Nicotinamide API manufacturers, exporters, distributors and traders.
click here to find a list of Nicotinamide suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Nicotinamide Drug Master File in Japan (Nicotinamide JDMF) empowers Nicotinamide 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 Nicotinamide JDMF during the approval evaluation for pharmaceutical products. At the time of Nicotinamide 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 Nicotinamide suppliers with JDMF on PharmaCompass.
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