01 1Kyowa Hakko Bio Co., Ltd.
02 1Toa Eiyo Co., Ltd.
01 1Flavin adenine dinucleotide sodium
02 1Japanese Pharmacopoeia flavin adenine dinucleotide sodium (production only)
01 2Japan
Japanese Pharmacopoeia Flavin Adenine Dinucleotide Sodium (For manufacturing purposes only)
Registration Number : 217MF10264
Registrant's Address : 1-6-1 Otemachi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-06-15
Latest Date of Registration : 2006-06-09
Flavin adenine dinucleotide sodium salt
Registration Number : 217MF10550
Registrant's Address : 3-1-2 Kyobashi, Chuo-ku, Tokyo
Initial Date of Registration : 2005-09-09
Latest Date of Registration : 2007-03-14
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PharmaCompass offers a list of Acetylpyridine Adenine Dinucleotide 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 Acetylpyridine Adenine Dinucleotide manufacturer or Acetylpyridine Adenine Dinucleotide supplier for your needs.
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PharmaCompass also assists you with knowing the Acetylpyridine Adenine Dinucleotide API Price utilized in the formulation of products. Acetylpyridine Adenine Dinucleotide API Price is not always fixed or binding as the Acetylpyridine Adenine Dinucleotide Price is obtained through a variety of data sources. The Acetylpyridine Adenine Dinucleotide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A APADH manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of APADH, including repackagers and relabelers. The FDA regulates APADH manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. APADH API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A APADH supplier is an individual or a company that provides APADH active pharmaceutical ingredient (API) or APADH finished formulations upon request. The APADH suppliers may include APADH 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 APADH Drug Master File in Japan (APADH JDMF) empowers APADH 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 APADH JDMF during the approval evaluation for pharmaceutical products. At the time of APADH JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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