01 1Ace Japan Co., Ltd.
01 1Pasotomin
01 1Japan
Registration Number : 217MF11241
Registrant's Address : 5850-1 Higashine-ko, Higashine City, Yamagata Prefecture
Initial Date of Registration : 2005-12-20
Latest Date of Registration : 2010-03-09
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PharmaCompass offers a list of Prochlorperazine Maleate 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 Prochlorperazine Maleate manufacturer or Prochlorperazine Maleate supplier for your needs.
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PharmaCompass also assists you with knowing the Prochlorperazine Maleate API Price utilized in the formulation of products. Prochlorperazine Maleate API Price is not always fixed or binding as the Prochlorperazine Maleate Price is obtained through a variety of data sources. The Prochlorperazine Maleate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Prochlorperazine Maleate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prochlorperazine Maleate, including repackagers and relabelers. The FDA regulates Prochlorperazine Maleate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prochlorperazine Maleate 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 Prochlorperazine Maleate supplier is an individual or a company that provides Prochlorperazine Maleate active pharmaceutical ingredient (API) or Prochlorperazine Maleate finished formulations upon request. The Prochlorperazine Maleate suppliers may include Prochlorperazine Maleate API manufacturers, exporters, distributors and traders.
click here to find a list of Prochlorperazine Maleate 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 Prochlorperazine Maleate Drug Master File in Japan (Prochlorperazine Maleate JDMF) empowers Prochlorperazine Maleate 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 Prochlorperazine Maleate JDMF during the approval evaluation for pharmaceutical products. At the time of Prochlorperazine Maleate 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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