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