01 1Daito Co., Ltd.
02 1Sanyo Chemical Research Institute Co., Ltd.
03 1Yoshindo Co., Ltd.
01 2Azelastine hydrochloride
02 1Day stations azelastine hydrochloride (production only)
01 1Gabon
02 2Japan
JP 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 : 220MF10046
Registrant's Address : 148-1 Tajii, Mihara-ku, Sakai City, Osaka Prefecture
Initial Date of Registration : 2008-02-05
Latest Date of Registration : 2008-02-05
Registration Number : 218MF10125
Registrant's Address : 3697-8 Hagishima, Funauchi-cho, Toyama City, Toyama Prefecture
Initial Date of Registration : 2006-01-30
Latest Date of Registration : 2009-11-09
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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 Azep manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Azep, including repackagers and relabelers. The FDA regulates Azep manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Azep 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 Azep manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Azep supplier is an individual or a company that provides Azep active pharmaceutical ingredient (API) or Azep finished formulations upon request. The Azep suppliers may include Azep API manufacturers, exporters, distributors and traders.
click here to find a list of Azep 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 Azep Drug Master File in Japan (Azep JDMF) empowers Azep 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 Azep JDMF during the approval evaluation for pharmaceutical products. At the time of Azep 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 Azep suppliers with JDMF on PharmaCompass.
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