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01 Changzhou Sunlight Pharmaceutical Co. , Ltd. (1)
01 Ethyl benzoate (1)
01 China (1)
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PharmaCompass offers a list of Benzocaine 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 Benzocaine manufacturer or Benzocaine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Benzocaine manufacturer or Benzocaine supplier.
PharmaCompass also assists you with knowing the Benzocaine API Price utilized in the formulation of products. Benzocaine API Price is not always fixed or binding as the Benzocaine Price is obtained through a variety of data sources. The Benzocaine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 06952_FLUKA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 06952_FLUKA, including repackagers and relabelers. The FDA regulates 06952_FLUKA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 06952_FLUKA 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 06952_FLUKA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 06952_FLUKA supplier is an individual or a company that provides 06952_FLUKA active pharmaceutical ingredient (API) or 06952_FLUKA finished formulations upon request. The 06952_FLUKA suppliers may include 06952_FLUKA API manufacturers, exporters, distributors and traders.
click here to find a list of 06952_FLUKA 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 06952_FLUKA Drug Master File in Japan (06952_FLUKA JDMF) empowers 06952_FLUKA 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 06952_FLUKA JDMF during the approval evaluation for pharmaceutical products. At the time of 06952_FLUKA 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 06952_FLUKA suppliers with JDMF on PharmaCompass.
We have 1 companies offering 06952_FLUKA
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