01 1Daito Co., Ltd.
02 1Yoshindo Co., Ltd.
01 1Azelastine hydrochloride
02 1Day stations azelastine hydrochloride (production only)
01 2Japan
Japanese Pharmacopoeia Azelastine Hydrochloride (for manufacturing purposes only)
Registration Number : 221MF10060
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2009-03-19
Latest Date of Registration : 2009-03-19
Registration Number : 218MF10125
Registrant's Address : 3697-8 Hagishima, Funamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2006-01-30
Latest Date of Registration : 2009-11-09
79
PharmaCompass offers a list of Azelastine 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 Azelastine Hydrochloride manufacturer or Azelastine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Azelastine Hydrochloride manufacturer or Azelastine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Azelastine Hydrochloride API Price utilized in the formulation of products. Azelastine Hydrochloride API Price is not always fixed or binding as the Azelastine Hydrochloride Price is obtained through a variety of data sources. The Azelastine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vividrin akut Azelastin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vividrin akut Azelastin, including repackagers and relabelers. The FDA regulates Vividrin akut Azelastin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vividrin akut Azelastin 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 Vividrin akut Azelastin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vividrin akut Azelastin supplier is an individual or a company that provides Vividrin akut Azelastin active pharmaceutical ingredient (API) or Vividrin akut Azelastin finished formulations upon request. The Vividrin akut Azelastin suppliers may include Vividrin akut Azelastin API manufacturers, exporters, distributors and traders.
click here to find a list of Vividrin akut Azelastin 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 Vividrin akut Azelastin Drug Master File in Japan (Vividrin akut Azelastin JDMF) empowers Vividrin akut Azelastin 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 Vividrin akut Azelastin JDMF during the approval evaluation for pharmaceutical products. At the time of Vividrin akut Azelastin 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 Vividrin akut Azelastin suppliers with JDMF on PharmaCompass.
We have 2 companies offering Vividrin akut Azelastin
Get in contact with the supplier of your choice:
