01 1Hebei Guangxiang Pharmaceutical Co. , Ltd.
02 2Shandong Xinhua Pharmaceutical Co. , Ltd.
03 1Shizuoka Caffeine Industrial Co., Ltd.
04 1Yashiro Pharmaceutical Co., Ltd.
01 2Japanese Pharmacopoeia theophylline (production only)
02 2Theophylline
03 1Theophylline PT
01 3China
02 1Japan
03 1Blank
Registration Number : 304MF10162
Registrant's Address : The East of Jingliu Road, West of Cangzhou Lingang Economic and Technological Develop...
Initial Date of Registration : 2022-12-23
Latest Date of Registration : 2022-12-23
Japanese Pharmacopoeia Theophylline (for manufacturing purposes only)
Registration Number : 217MF10613
Registrant's Address : 129 Suido-cho, Aoi-ku, Shizuoka City, Shizuoka Prefecture
Initial Date of Registration : 2005-09-14
Latest Date of Registration : 2023-12-22
Registration Number : 219MF10215
Registrant's Address : No. 14 Dongyi Road, Zhangdian Zibo, Shandong, P. R. China
Initial Date of Registration : 2007-06-25
Latest Date of Registration : 2007-06-25
Japanese Pharmacopoeia Theophylline (for manufacturing purposes only)
Registration Number : 217MF10482
Registrant's Address : No. 1, Lutai Road, High-tech District, Zibo, Shandong, P. R. China
Initial Date of Registration : 2005-09-06
Latest Date of Registration : 2012-02-01
Registration Number : 218MF10248
Registrant's Address : 10-2 Yoshida Shimojima, Higashiosaka City, Osaka Prefecture
Initial Date of Registration : 2006-02-16
Latest Date of Registration : 2009-10-08
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PharmaCompass offers a list of Theophylline 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 Theophylline manufacturer or Theophylline supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Theophylline manufacturer or Theophylline supplier.
A Theograd manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Theograd, including repackagers and relabelers. The FDA regulates Theograd manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Theograd 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 Theograd manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Theograd supplier is an individual or a company that provides Theograd active pharmaceutical ingredient (API) or Theograd finished formulations upon request. The Theograd suppliers may include Theograd API manufacturers, exporters, distributors and traders.
click here to find a list of Theograd 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 Theograd Drug Master File in Japan (Theograd JDMF) empowers Theograd 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 Theograd JDMF during the approval evaluation for pharmaceutical products. At the time of Theograd 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 Theograd suppliers with JDMF on PharmaCompass.
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