01 Dishman Pharmaceuticals and Chemicals Limited (1)
02 Junsei Chemical Co., Ltd. (2)
03 Organo Syntesis, S. A. de C. V. (1)
01 Benzethonium chloride (2)
02 Japanese Pharmacopoeia benzethonium chloride (1)
03 Japanese Pharmacopoeia benzethonium chloride (production only) (1)
01 India (1)
02 Japan (2)
03 Mexico (1)
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PharmaCompass offers a list of Benzethonium Chloride 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 Benzethonium Chloride manufacturer or Benzethonium Chloride supplier for your needs.
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PharmaCompass also assists you with knowing the Benzethonium Chloride API Price utilized in the formulation of products. Benzethonium Chloride API Price is not always fixed or binding as the Benzethonium Chloride Price is obtained through a variety of data sources. The Benzethonium Chloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tox21_202488 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_202488, including repackagers and relabelers. The FDA regulates Tox21_202488 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_202488 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 Tox21_202488 supplier is an individual or a company that provides Tox21_202488 active pharmaceutical ingredient (API) or Tox21_202488 finished formulations upon request. The Tox21_202488 suppliers may include Tox21_202488 API manufacturers, exporters, distributors and traders.
click here to find a list of Tox21_202488 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 Tox21_202488 Drug Master File in Japan (Tox21_202488 JDMF) empowers Tox21_202488 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 Tox21_202488 JDMF during the approval evaluation for pharmaceutical products. At the time of Tox21_202488 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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