01 1Daito Co., Ltd.
01 1Day stations arotinolol hydrochloride (production only)
01 1Japan
JP Arotinolol Hydrochloride (For manufacturing only)
Registration Number : 219MF10032
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2007-02-05
Latest Date of Registration : 2016-08-29
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PharmaCompass offers a list of Arotinolol 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 Arotinolol Hydrochloride manufacturer or Arotinolol Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Arotinolol Hydrochloride manufacturer or Arotinolol Hydrochloride supplier.
PharmaCompass also assists you with knowing the Arotinolol Hydrochloride API Price utilized in the formulation of products. Arotinolol Hydrochloride API Price is not always fixed or binding as the Arotinolol Hydrochloride Price is obtained through a variety of data sources. The Arotinolol Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Arotinolol Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Arotinolol Hydrochloride, including repackagers and relabelers. The FDA regulates Arotinolol Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Arotinolol 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 Arotinolol Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Arotinolol Hydrochloride supplier is an individual or a company that provides Arotinolol Hydrochloride active pharmaceutical ingredient (API) or Arotinolol Hydrochloride finished formulations upon request. The Arotinolol Hydrochloride suppliers may include Arotinolol Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Arotinolol 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 Arotinolol Hydrochloride Drug Master File in Japan (Arotinolol Hydrochloride JDMF) empowers Arotinolol 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 Arotinolol Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Arotinolol 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 Arotinolol Hydrochloride suppliers with JDMF on PharmaCompass.
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