Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1MOEHS IBERICA S. L.
02 1Ipca Laboratories Limited
03 1Speranexus Co., Ltd.
01 3Metoprolol tartrate
01 1India
02 1Japan
03 1Spain
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Registration Number : 222MF10104
Registrant's Address : Cesar Martinell i Brunet 12A, Poligono Rubi Sur, Rubi (Barcelona), Spain
Initial Date of Registration : 2010-03-18
Latest Date of Registration : 2019-03-11
Registration Number : 221MF10151
Registrant's Address : 48, Kandivli Industrial Estate, Kandivli (W), Mumbai 400 067, INDIA
Initial Date of Registration : 2009-07-09
Latest Date of Registration : 2009-07-09
Registration Number : 217MF10047
Registrant's Address : 4-8-2 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-05-20
Latest Date of Registration : 2008-01-10
99
PharmaCompass offers a list of Metoprolol Tartrate 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 Metoprolol Tartrate manufacturer or Metoprolol Tartrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Metoprolol Tartrate manufacturer or Metoprolol Tartrate supplier.
A CS-3159 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CS-3159, including repackagers and relabelers. The FDA regulates CS-3159 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CS-3159 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 CS-3159 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A CS-3159 supplier is an individual or a company that provides CS-3159 active pharmaceutical ingredient (API) or CS-3159 finished formulations upon request. The CS-3159 suppliers may include CS-3159 API manufacturers, exporters, distributors and traders.
click here to find a list of CS-3159 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 CS-3159 Drug Master File in Japan (CS-3159 JDMF) empowers CS-3159 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 CS-3159 JDMF during the approval evaluation for pharmaceutical products. At the time of CS-3159 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 CS-3159 suppliers with JDMF on PharmaCompass.
We have 3 companies offering CS-3159
Get in contact with the supplier of your choice:
