01 1Edmond Pharma s. r. l.
02 1Sanbo Chemical Industry Co., Ltd.
03 1Shaanxi Dasheng Pharmaceutical Tech Co. , Ltd.
01 1Procaterol Hydrochloride
02 1Procaterol hydrochloride hydrate
03 1Procaterol hydrochloride hydrate (production only)
01 1China
02 1Japan
03 1Sweden
Procaterol hydrochloride hydrate (for manufacturing purposes only)
Registration Number : 220MF10003
Registrant's Address : 7-30-7 Toshima, Kita-ku, Tokyo
Initial Date of Registration : 2008-01-09
Latest Date of Registration : 2008-01-09
Procaterol hydrochloride hydrate
Registration Number : 218MF10948
Registrant's Address : Strada Statale dei Giovi, 131-20037 Paderno Dugnano (MI) - Italy
Initial Date of Registration : 2006-11-24
Latest Date of Registration : 2010-04-14
Procaterol hydrochloride hydrate
Registration Number : 306MF10056
Registrant's Address : F9 of Jiezuo Square, No. 2 South Fenghui Road, Xi'an Hi-Tech Industrial Development, ...
Initial Date of Registration : 2024-04-18
Latest Date of Registration : 2024-04-18
100
PharmaCompass offers a list of Procaterol API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Procaterol manufacturer or Procaterol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Procaterol manufacturer or Procaterol supplier.
A CI888 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CI888, including repackagers and relabelers. The FDA regulates CI888 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CI888 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 CI888 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A CI888 supplier is an individual or a company that provides CI888 active pharmaceutical ingredient (API) or CI888 finished formulations upon request. The CI888 suppliers may include CI888 API manufacturers, exporters, distributors and traders.
click here to find a list of CI888 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 CI888 Drug Master File in Japan (CI888 JDMF) empowers CI888 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 CI888 JDMF during the approval evaluation for pharmaceutical products. At the time of CI888 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 CI888 suppliers with JDMF on PharmaCompass.
We have 3 companies offering CI888
Get in contact with the supplier of your choice:
