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