01 1Kawaken Fine Chemicals Co., Ltd.
02 1Olon S. p. A.
01 1Japanese Pharmacopoeia di Memoru fan phosphate
02 1TRETINOIN type 2
01 1Italy
02 1Japan
Japanese Pharmacopoeia Dimemorfan Phosphate
Registration Number : 219MF10174
Registrant's Address : 2-3-3 Nihonbashi Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2007-06-01
Latest Date of Registration : 2007-06-01
Registration Number : 229MF10001
Registrant's Address : Strada Rivoltana, km 6/7, 20053 Rodano (MI), Italy
Initial Date of Registration : 2017-01-10
Latest Date of Registration : 2022-12-15
A Tretinoin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tretinoin, including repackagers and relabelers. The FDA regulates Tretinoin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tretinoin 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 Tretinoin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tretinoin supplier is an individual or a company that provides Tretinoin active pharmaceutical ingredient (API) or Tretinoin finished formulations upon request. The Tretinoin suppliers may include Tretinoin API manufacturers, exporters, distributors and traders.
click here to find a list of Tretinoin 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 Tretinoin Drug Master File in Japan (Tretinoin JDMF) empowers Tretinoin 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 Tretinoin JDMF during the approval evaluation for pharmaceutical products. At the time of Tretinoin 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 Tretinoin suppliers with JDMF on PharmaCompass.
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