01 2Cheer Fine Pharmaceutical Co. , Ltd.
02 1Daiwa Pharmaceutical Industries Co., Ltd.
03 1IcromS. r. l.
01 1Japan Bureau Sulpiride (for manufacturing only)
02 1Japanese Pharmacopoeia Drug sulpiride (production only)
03 1SULPIRIDE
04 1SULPIRIDE JP
01 2China
02 1India
03 1Italy
Registration Number : 220MF10210
Registrant's Address : No. 2066 Tangkou Road, Economy and Technology Development Zone, Hefei, Anhui Province...
Initial Date of Registration : 2008-09-30
Latest Date of Registration : 2008-10-17
Registration Number : 229MF10008
Registrant's Address : No. 2066 Tangkou Road, Economy and Technology Development Zone, Hefei, Anhui Province...
Initial Date of Registration : 2017-01-10
Latest Date of Registration : 2017-01-10
Japanese Pharmacopoeia Drug Sulpiride (for manufacturing only)
Registration Number : 217MF10507
Registrant's Address : 2-3-5 Shimookui, Toyama City, Toyama Prefecture
Initial Date of Registration : 2005-09-06
Latest Date of Registration : 2007-04-27
Japanese Pharmacopoeia Sulpiride (for manufacturing purposes only)
Registration Number : 218MF10084
Registrant's Address : Via Delle Arti 33, 20863 Concorezzo (MB), Italy
Initial Date of Registration : 2006-01-27
Latest Date of Registration : 2018-10-23
21
PharmaCompass offers a list of Sulpiride 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 Sulpiride manufacturer or Sulpiride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sulpiride manufacturer or Sulpiride supplier.
PharmaCompass also assists you with knowing the Sulpiride API Price utilized in the formulation of products. Sulpiride API Price is not always fixed or binding as the Sulpiride Price is obtained through a variety of data sources. The Sulpiride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Meresa manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Meresa, including repackagers and relabelers. The FDA regulates Meresa manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Meresa 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 Meresa manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Meresa supplier is an individual or a company that provides Meresa active pharmaceutical ingredient (API) or Meresa finished formulations upon request. The Meresa suppliers may include Meresa API manufacturers, exporters, distributors and traders.
click here to find a list of Meresa 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 Meresa Drug Master File in Japan (Meresa JDMF) empowers Meresa 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 Meresa JDMF during the approval evaluation for pharmaceutical products. At the time of Meresa 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 Meresa suppliers with JDMF on PharmaCompass.
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