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.
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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 Amben ethyl ester manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Amben ethyl ester, including repackagers and relabelers. The FDA regulates Amben ethyl ester manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Amben ethyl ester 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 Amben ethyl ester supplier is an individual or a company that provides Amben ethyl ester active pharmaceutical ingredient (API) or Amben ethyl ester finished formulations upon request. The Amben ethyl ester suppliers may include Amben ethyl ester API manufacturers, exporters, distributors and traders.
click here to find a list of Amben ethyl ester 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 Amben ethyl ester Drug Master File in Japan (Amben ethyl ester JDMF) empowers Amben ethyl ester 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 Amben ethyl ester JDMF during the approval evaluation for pharmaceutical products. At the time of Amben ethyl ester 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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