01 1Daito Co., Ltd.
02 1Yoshindo Co., Ltd.
01 1Azelastine hydrochloride
02 1Day stations azelastine hydrochloride (production only)
01 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 : 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.
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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 Optivar manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Optivar, including repackagers and relabelers. The FDA regulates Optivar manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Optivar 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 Optivar manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Optivar supplier is an individual or a company that provides Optivar active pharmaceutical ingredient (API) or Optivar finished formulations upon request. The Optivar suppliers may include Optivar API manufacturers, exporters, distributors and traders.
click here to find a list of Optivar 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 Optivar Drug Master File in Japan (Optivar JDMF) empowers Optivar 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 Optivar JDMF during the approval evaluation for pharmaceutical products. At the time of Optivar 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 Optivar suppliers with JDMF on PharmaCompass.
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