01 1SperaNexus Co., Ltd.
01 1Phenylephrine hydrochloride
01 1Japan
Registration Number : 217MF10030
Registrant's Address : 4-8-2 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-05-20
Latest Date of Registration : 2007-04-27
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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.
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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 VAZCULEP manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of VAZCULEP, including repackagers and relabelers. The FDA regulates VAZCULEP manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. VAZCULEP 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 VAZCULEP supplier is an individual or a company that provides VAZCULEP active pharmaceutical ingredient (API) or VAZCULEP finished formulations upon request. The VAZCULEP suppliers may include VAZCULEP API manufacturers, exporters, distributors and traders.
click here to find a list of VAZCULEP 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 VAZCULEP Drug Master File in Japan (VAZCULEP JDMF) empowers VAZCULEP 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 VAZCULEP JDMF during the approval evaluation for pharmaceutical products. At the time of VAZCULEP 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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