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
A Tropicamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tropicamide, including repackagers and relabelers. The FDA regulates Tropicamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tropicamide 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 Tropicamide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tropicamide supplier is an individual or a company that provides Tropicamide active pharmaceutical ingredient (API) or Tropicamide finished formulations upon request. The Tropicamide suppliers may include Tropicamide API manufacturers, exporters, distributors and traders.
click here to find a list of Tropicamide 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 Tropicamide Drug Master File in Japan (Tropicamide JDMF) empowers Tropicamide 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 Tropicamide JDMF during the approval evaluation for pharmaceutical products. At the time of Tropicamide 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 Tropicamide suppliers with JDMF on PharmaCompass.
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