01 2Lundbeck Pharmaceuticals Italy S. p. A
02 1Lusochimica S. p. A.
01 3Ritodrine hydrochloride
01 2Denmark
02 1Italy
Registration Number : 224MF10226
Registrant's Address : Via Quarta Strada, 2 Padova, Italy
Initial Date of Registration : 2012-12-06
Latest Date of Registration : 2012-12-06
Registration Number : 218MF10513
Registrant's Address : Via Quarta Strada, 2 Padova ITALY
Initial Date of Registration : 2006-05-18
Latest Date of Registration : 2006-05-18
Registration Number : 217MF11180
Registrant's Address : Via Giotto 9,23871 Lomagna(LC)Italy
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2021-05-17
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PharmaCompass offers a list of Ritodrine Hydrochloride 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 Ritodrine Hydrochloride manufacturer or Ritodrine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ritodrine Hydrochloride manufacturer or Ritodrine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Ritodrine Hydrochloride API Price utilized in the formulation of products. Ritodrine Hydrochloride API Price is not always fixed or binding as the Ritodrine Hydrochloride Price is obtained through a variety of data sources. The Ritodrine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Utopar manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Utopar, including repackagers and relabelers. The FDA regulates Utopar manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Utopar 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 Utopar manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Utopar supplier is an individual or a company that provides Utopar active pharmaceutical ingredient (API) or Utopar finished formulations upon request. The Utopar suppliers may include Utopar API manufacturers, exporters, distributors and traders.
click here to find a list of Utopar 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 Utopar Drug Master File in Japan (Utopar JDMF) empowers Utopar 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 Utopar JDMF during the approval evaluation for pharmaceutical products. At the time of Utopar 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 Utopar suppliers with JDMF on PharmaCompass.
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