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
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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, Price,and more, enabling you to easily find the right Tretinoin manufacturer or Tretinoin supplier for your needs.
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A Cordes vas manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cordes vas, including repackagers and relabelers. The FDA regulates Cordes vas manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cordes vas API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Cordes vas supplier is an individual or a company that provides Cordes vas active pharmaceutical ingredient (API) or Cordes vas finished formulations upon request. The Cordes vas suppliers may include Cordes vas API manufacturers, exporters, distributors and traders.
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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 Cordes vas Drug Master File in Japan (Cordes vas JDMF) empowers Cordes vas API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
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