01 1Shandong Xinhua Pharmaceutical Co. , Ltd.
02 1Yashiro Pharmaceutical Co., Ltd.
01 2Aminophylline hydrate
01 1China
02 1Blank
Registration Number : 307MF10141
Registrant's Address : No. 1, Lutai Road, High-tech District, Zibo, Shandong, P. R. China
Initial Date of Registration : 2025-11-26
Latest Date of Registration : 2025-11-26
Registration Number : 222MF10082
Registrant's Address : 10-2 Yoshida Shimojima, Higashiosaka City, Osaka Prefecture
Initial Date of Registration : 2010-03-09
Latest Date of Registration : 2010-03-09
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PharmaCompass offers a list of Aminophylline 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 Aminophylline manufacturer or Aminophylline supplier for your needs.
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PharmaCompass also assists you with knowing the Aminophylline API Price utilized in the formulation of products. Aminophylline API Price is not always fixed or binding as the Aminophylline Price is obtained through a variety of data sources. The Aminophylline Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Etilen-xantisan tabl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Etilen-xantisan tabl, including repackagers and relabelers. The FDA regulates Etilen-xantisan tabl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Etilen-xantisan tabl API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Etilen-xantisan tabl supplier is an individual or a company that provides Etilen-xantisan tabl active pharmaceutical ingredient (API) or Etilen-xantisan tabl finished formulations upon request. The Etilen-xantisan tabl suppliers may include Etilen-xantisan tabl API manufacturers, exporters, distributors and traders.
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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 Etilen-xantisan tabl Drug Master File in Japan (Etilen-xantisan tabl JDMF) empowers Etilen-xantisan tabl 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 Etilen-xantisan tabl JDMF during the approval evaluation for pharmaceutical products. At the time of Etilen-xantisan tabl JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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