01 1Daito Co., Ltd.
02 1Kanto Chemical Co., Ltd.
01 1Carteolol hydrochloride salt
02 1Day stations carteolol hydrochloride (production only)
01 2Japan
JP Carteolol Hydrochloride (for manufacturing purposes only)
Registration Number : 219MF10024
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2007-01-22
Latest Date of Registration : 2007-01-22
Registration Number : 221MF10036
Registrant's Address : 3-2-8 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2009-02-09
Latest Date of Registration : 2009-02-09
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PharmaCompass offers a list of Carteolol 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 Carteolol manufacturer or Carteolol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Carteolol manufacturer or Carteolol supplier.
PharmaCompass also assists you with knowing the Carteolol API Price utilized in the formulation of products. Carteolol API Price is not always fixed or binding as the Carteolol Price is obtained through a variety of data sources. The Carteolol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ocupress manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ocupress, including repackagers and relabelers. The FDA regulates Ocupress manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ocupress 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 Ocupress manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ocupress supplier is an individual or a company that provides Ocupress active pharmaceutical ingredient (API) or Ocupress finished formulations upon request. The Ocupress suppliers may include Ocupress API manufacturers, exporters, distributors and traders.
click here to find a list of Ocupress 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 Ocupress Drug Master File in Japan (Ocupress JDMF) empowers Ocupress 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 Ocupress JDMF during the approval evaluation for pharmaceutical products. At the time of Ocupress 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 Ocupress suppliers with JDMF on PharmaCompass.
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