01 1Aurobindo Pharma Limited
02 1YS Life Science Co. , Ltd.
01 2Pramipexole hydrochloride hydrate
01 1India
02 1South Korea
Pramipexole hydrochloride hydrate
Registration Number : 223MF10156
Registrant's Address : Plot No. 2, Maitrivihar, Ameerpet, Hyderabad Andhra Pradesh, India
Initial Date of Registration : 2011-11-02
Latest Date of Registration : 2012-10-31
Pramipexole hydrochloride hydrate
Registration Number : 223MF10181
Registrant's Address : 207, Sujeong-ro, Jangan-myeon, Hwaseong-si, Gyeonggi-do, 18581, Republic of Korea
Initial Date of Registration : 2011-12-27
Latest Date of Registration : 2021-11-02
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PharmaCompass offers a list of Pramipexole Dihydrochloride 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 Pramipexole Dihydrochloride manufacturer or Pramipexole Dihydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pramipexole Dihydrochloride manufacturer or Pramipexole Dihydrochloride supplier.
PharmaCompass also assists you with knowing the Pramipexole Dihydrochloride API Price utilized in the formulation of products. Pramipexole Dihydrochloride API Price is not always fixed or binding as the Pramipexole Dihydrochloride Price is obtained through a variety of data sources. The Pramipexole Dihydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sifrol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sifrol, including repackagers and relabelers. The FDA regulates Sifrol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sifrol 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 Sifrol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sifrol supplier is an individual or a company that provides Sifrol active pharmaceutical ingredient (API) or Sifrol finished formulations upon request. The Sifrol suppliers may include Sifrol API manufacturers, exporters, distributors and traders.
click here to find a list of Sifrol 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 Sifrol Drug Master File in Japan (Sifrol JDMF) empowers Sifrol 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 Sifrol JDMF during the approval evaluation for pharmaceutical products. At the time of Sifrol 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 Sifrol suppliers with JDMF on PharmaCompass.
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