01 1Kongo Chemical Co., Ltd.
01 1Diphenhydramine hydrochloride (production only)
01 1Japan
Diphenhydramine hydrochloride (for manufacturing purposes only)
Registration Number : 217MF11188
Registrant's Address : 3 Himata, Toyama City, Toyama Prefecture
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2010-03-09
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PharmaCompass offers a list of Diphenhydramine 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 Diphenhydramine Hydrochloride manufacturer or Diphenhydramine Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Diphenhydramine Hydrochloride API Price utilized in the formulation of products. Diphenhydramine Hydrochloride API Price is not always fixed or binding as the Diphenhydramine Hydrochloride Price is obtained through a variety of data sources. The Diphenhydramine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A IBUPROFEN AND DIPHENHYDRAMINE HYDROCHLORIDE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of IBUPROFEN AND DIPHENHYDRAMINE HYDROCHLORIDE, including repackagers and relabelers. The FDA regulates IBUPROFEN AND DIPHENHYDRAMINE HYDROCHLORIDE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. IBUPROFEN AND DIPHENHYDRAMINE 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.
click here to find a list of IBUPROFEN AND DIPHENHYDRAMINE HYDROCHLORIDE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A IBUPROFEN AND DIPHENHYDRAMINE HYDROCHLORIDE supplier is an individual or a company that provides IBUPROFEN AND DIPHENHYDRAMINE HYDROCHLORIDE active pharmaceutical ingredient (API) or IBUPROFEN AND DIPHENHYDRAMINE HYDROCHLORIDE finished formulations upon request. The IBUPROFEN AND DIPHENHYDRAMINE HYDROCHLORIDE suppliers may include IBUPROFEN AND DIPHENHYDRAMINE HYDROCHLORIDE API manufacturers, exporters, distributors and traders.
click here to find a list of IBUPROFEN AND DIPHENHYDRAMINE 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 IBUPROFEN AND DIPHENHYDRAMINE HYDROCHLORIDE Drug Master File in Japan (IBUPROFEN AND DIPHENHYDRAMINE HYDROCHLORIDE JDMF) empowers IBUPROFEN AND DIPHENHYDRAMINE 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 IBUPROFEN AND DIPHENHYDRAMINE HYDROCHLORIDE JDMF during the approval evaluation for pharmaceutical products. At the time of IBUPROFEN AND DIPHENHYDRAMINE 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 IBUPROFEN AND DIPHENHYDRAMINE HYDROCHLORIDE suppliers with JDMF on PharmaCompass.
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