01 1Minsheng Group Shaoxing Pharmaceutical Co. , Ltd.
02 1Tokyo Chemical Industry Co., Ltd.
01 2Tropicamide
01 1China
02 1Japan
Registration Number : 306MF10111
Registrant's Address : 315, Tanggong Road, Paojiang Industrial Zone, Shaoxing, P. R. China
Initial Date of Registration : 2024-08-07
Latest Date of Registration : 2024-08-07
Registration Number : 217MF11157
Registrant's Address : 6-15-9 Toshima, Kita-ku, Tokyo
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2020-10-05
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PharmaCompass offers a list of Tropicamide 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 Tropicamide manufacturer or Tropicamide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tropicamide manufacturer or Tropicamide supplier.
PharmaCompass also assists you with knowing the Tropicamide API Price utilized in the formulation of products. Tropicamide API Price is not always fixed or binding as the Tropicamide Price is obtained through a variety of data sources. The Tropicamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Mydrum manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mydrum, including repackagers and relabelers. The FDA regulates Mydrum manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mydrum 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 Mydrum manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mydrum supplier is an individual or a company that provides Mydrum active pharmaceutical ingredient (API) or Mydrum finished formulations upon request. The Mydrum suppliers may include Mydrum API manufacturers, exporters, distributors and traders.
click here to find a list of Mydrum 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 Mydrum Drug Master File in Japan (Mydrum JDMF) empowers Mydrum 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 Mydrum JDMF during the approval evaluation for pharmaceutical products. At the time of Mydrum 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 Mydrum suppliers with JDMF on PharmaCompass.
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