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 : 8-1 Higashinakagawara, Segami-cho, Fukushima City, Fukushima Prefecture
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.
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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 DIPTA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DIPTA, including repackagers and relabelers. The FDA regulates DIPTA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DIPTA 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 DIPTA supplier is an individual or a company that provides DIPTA active pharmaceutical ingredient (API) or DIPTA finished formulations upon request. The DIPTA suppliers may include DIPTA API manufacturers, exporters, distributors and traders.
click here to find a list of DIPTA 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 DIPTA Drug Master File in Japan (DIPTA JDMF) empowers DIPTA 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 DIPTA JDMF during the approval evaluation for pharmaceutical products. At the time of DIPTA 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 DIPTA suppliers with JDMF on PharmaCompass.
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