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PharmaCompass offers a list of Phenylephrine Hydrochloride 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 Phenylephrine Hydrochloride manufacturer or Phenylephrine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Phenylephrine Hydrochloride manufacturer or Phenylephrine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Phenylephrine Hydrochloride API Price utilized in the formulation of products. Phenylephrine Hydrochloride API Price is not always fixed or binding as the Phenylephrine Hydrochloride Price is obtained through a variety of data sources. The Phenylephrine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 04JA59TNSJ manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 04JA59TNSJ, including repackagers and relabelers. The FDA regulates 04JA59TNSJ manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 04JA59TNSJ 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 04JA59TNSJ manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 04JA59TNSJ supplier is an individual or a company that provides 04JA59TNSJ active pharmaceutical ingredient (API) or 04JA59TNSJ finished formulations upon request. The 04JA59TNSJ suppliers may include 04JA59TNSJ API manufacturers, exporters, distributors and traders.
click here to find a list of 04JA59TNSJ 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 04JA59TNSJ Drug Master File in Japan (04JA59TNSJ JDMF) empowers 04JA59TNSJ 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 04JA59TNSJ JDMF during the approval evaluation for pharmaceutical products. At the time of 04JA59TNSJ 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 04JA59TNSJ suppliers with JDMF on PharmaCompass.
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