01 1Dojin Pharmaceutical Chemical Co., Ltd.
02 1Sicor de Me(´)xico,S. A. de C. V.
01 1Deployed Don propionate "Teva"
02 1Deprodone propionic acid
01 1Japan
02 1Mexico
Registration Number : 217MF10385
Registrant's Address : Fukushima Prefecture, Fukushima City, Segami Town, Higashi Nakagawara 8-1
Initial Date of Registration : 2005-07-27
Latest Date of Registration : 2011-12-09
Registration Number : 218MF10927
Registrant's Address : Av. San Rafael No. 35 Parque Industrial Lerma, CP52000 Lerma, Edo. Me(´)xico. MEXICO
Initial Date of Registration : 2006-11-21
Latest Date of Registration : 2006-11-21
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PharmaCompass offers a list of 3-5-Diiodothyropropionic Acid 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 3-5-Diiodothyropropionic Acid manufacturer or 3-5-Diiodothyropropionic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred 3-5-Diiodothyropropionic Acid manufacturer or 3-5-Diiodothyropropionic Acid supplier.
PharmaCompass also assists you with knowing the 3-5-Diiodothyropropionic Acid API Price utilized in the formulation of products. 3-5-Diiodothyropropionic Acid API Price is not always fixed or binding as the 3-5-Diiodothyropropionic Acid Price is obtained through a variety of data sources. The 3-5-Diiodothyropropionic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dipro manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dipro, including repackagers and relabelers. The FDA regulates Dipro manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dipro API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Dipro supplier is an individual or a company that provides Dipro active pharmaceutical ingredient (API) or Dipro finished formulations upon request. The Dipro suppliers may include Dipro API manufacturers, exporters, distributors and traders.
click here to find a list of Dipro 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 Dipro Drug Master File in Japan (Dipro JDMF) empowers Dipro 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 Dipro JDMF during the approval evaluation for pharmaceutical products. At the time of Dipro 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 Dipro suppliers with JDMF on PharmaCompass.
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