01 1Daito Co., Ltd.
01 1Day stations homochlorcyclizine hydrochloride (production only)
01 1Japan
JP Homochlorcyclizine Hydrochloride (for manufacturing only)
Registration Number : 218MF10887
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2006-11-10
Latest Date of Registration : 2006-11-10
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PharmaCompass offers a list of Homochlorcyclizine 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 Homochlorcyclizine Hydrochloride manufacturer or Homochlorcyclizine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Homochlorcyclizine Hydrochloride manufacturer or Homochlorcyclizine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Homochlorcyclizine Hydrochloride API Price utilized in the formulation of products. Homochlorcyclizine Hydrochloride API Price is not always fixed or binding as the Homochlorcyclizine Hydrochloride Price is obtained through a variety of data sources. The Homochlorcyclizine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Homochlorcyclizine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Homochlorcyclizine Hydrochloride, including repackagers and relabelers. The FDA regulates Homochlorcyclizine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Homochlorcyclizine Hydrochloride API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Homochlorcyclizine Hydrochloride supplier is an individual or a company that provides Homochlorcyclizine Hydrochloride active pharmaceutical ingredient (API) or Homochlorcyclizine Hydrochloride finished formulations upon request. The Homochlorcyclizine Hydrochloride suppliers may include Homochlorcyclizine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Homochlorcyclizine Hydrochloride 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 Homochlorcyclizine Hydrochloride Drug Master File in Japan (Homochlorcyclizine Hydrochloride JDMF) empowers Homochlorcyclizine Hydrochloride 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 Homochlorcyclizine Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Homochlorcyclizine Hydrochloride 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 Homochlorcyclizine Hydrochloride suppliers with JDMF on PharmaCompass.
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