01 2Kongo Chemical Co., Ltd.
01 1Diphenhydramine (production only)
02 1Salicylic acid diphenhydramine (production only)
01 2Japan
Diphenhydramine (for manufacturing purposes only)
Registration Number : 217MF11191
Registrant's Address : 3 Himata, Toyama City, Toyama Prefecture
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2021-04-13
Diphenhydramine salicylate (for manufacturing purposes only)
Registration Number : 217MF11205
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 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 manufacturer or Diphenhydramine supplier for your needs.
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PharmaCompass also assists you with knowing the Diphenhydramine API Price utilized in the formulation of products. Diphenhydramine API Price is not always fixed or binding as the Diphenhydramine Price is obtained through a variety of data sources. The Diphenhydramine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Benylin Chesty Coughs Original manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Benylin Chesty Coughs Original, including repackagers and relabelers. The FDA regulates Benylin Chesty Coughs Original manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Benylin Chesty Coughs Original 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 Benylin Chesty Coughs Original supplier is an individual or a company that provides Benylin Chesty Coughs Original active pharmaceutical ingredient (API) or Benylin Chesty Coughs Original finished formulations upon request. The Benylin Chesty Coughs Original suppliers may include Benylin Chesty Coughs Original API manufacturers, exporters, distributors and traders.
click here to find a list of Benylin Chesty Coughs Original 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 Benylin Chesty Coughs Original Drug Master File in Japan (Benylin Chesty Coughs Original JDMF) empowers Benylin Chesty Coughs Original 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 Benylin Chesty Coughs Original JDMF during the approval evaluation for pharmaceutical products. At the time of Benylin Chesty Coughs Original 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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