01 1Edmond Pharma s. r. l.
02 1LABORATORI ALCHEMIA SRL
03 1Ohara Pharmaceutical Co., Ltd.
01 1MIDODRINE HYDROCHLORIDE
02 1Midodrine hydrochloride
03 1Outsiders regulations midodrine hydrochloride (production only)
01 1Italy
02 1Japan
03 1Sweden
Registration Number : 221MF10211
Registrant's Address : Via San Faustino, 68 20134 MILANO-Italy
Initial Date of Registration : 2009-09-28
Latest Date of Registration : 2016-10-21
Midodrine Hydrochloride (for manufacturing purposes only)
Registration Number : 217MF11229
Registrant's Address : 121-15 Torino, Koka-cho, Koka City, Shiga Prefecture
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2008-10-10
Registration Number : 217MF10582
Registrant's Address : Strada Statale dei Giovi, 131-20037 Paderno Dugnano (MI) - Italy
Initial Date of Registration : 2005-09-14
Latest Date of Registration : 2021-02-19
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PharmaCompass offers a list of Midodrine 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 Midodrine manufacturer or Midodrine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Midodrine manufacturer or Midodrine supplier.
PharmaCompass also assists you with knowing the Midodrine API Price utilized in the formulation of products. Midodrine API Price is not always fixed or binding as the Midodrine Price is obtained through a variety of data sources. The Midodrine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Gutron manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gutron, including repackagers and relabelers. The FDA regulates Gutron manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gutron 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 Gutron manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Gutron supplier is an individual or a company that provides Gutron active pharmaceutical ingredient (API) or Gutron finished formulations upon request. The Gutron suppliers may include Gutron API manufacturers, exporters, distributors and traders.
click here to find a list of Gutron 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 Gutron Drug Master File in Japan (Gutron JDMF) empowers Gutron 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 Gutron JDMF during the approval evaluation for pharmaceutical products. At the time of Gutron 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 Gutron suppliers with JDMF on PharmaCompass.
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