01 1Changzhou Sunlight Pharmaceutical Co. , Ltd.
01 1Ethyl benzoate
01 1China
Registration Number : 229MF10006
Registrant's Address : No. 1 Honglou Road, Jiuli Street, Benniu Town, Xinbei District, Changzhou, Jiangsu Pr...
Initial Date of Registration : 2017-01-10
Latest Date of Registration : 2024-07-11
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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 Ethyl PABA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ethyl PABA, including repackagers and relabelers. The FDA regulates Ethyl PABA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ethyl PABA 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 Ethyl PABA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ethyl PABA supplier is an individual or a company that provides Ethyl PABA active pharmaceutical ingredient (API) or Ethyl PABA finished formulations upon request. The Ethyl PABA suppliers may include Ethyl PABA API manufacturers, exporters, distributors and traders.
click here to find a list of Ethyl PABA 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 Ethyl PABA Drug Master File in Japan (Ethyl PABA JDMF) empowers Ethyl PABA 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 Ethyl PABA JDMF during the approval evaluation for pharmaceutical products. At the time of Ethyl PABA 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 Ethyl PABA suppliers with JDMF on PharmaCompass.
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