01 1Lonza Guangzhou Pharmaceutical Ltd
01 1Nicotinic acid amide
01 1Switzerland
Registration Number : 226MF10200
Registrant's Address : No. 127, Building C1, No. 1 Qingsheng Avenue, Nansha District, Guangzhou, PRC
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 N0078 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of N0078, including repackagers and relabelers. The FDA regulates N0078 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. N0078 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A N0078 supplier is an individual or a company that provides N0078 active pharmaceutical ingredient (API) or N0078 finished formulations upon request. The N0078 suppliers may include N0078 API manufacturers, exporters, distributors and traders.
click here to find a list of N0078 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 N0078 Drug Master File in Japan (N0078 JDMF) empowers N0078 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 N0078 JDMF during the approval evaluation for pharmaceutical products. At the time of N0078 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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