01 1Heraeus Precious Metals GmbH & Co. K.G.
02 1Nippon Rika Pharmaceuticals Co., Ltd.
01 15-Aminolevulinic acid hydrochloride
02 1Aminolevulinic acid hydrochloride salt
01 1Germany
02 1Japan
5-Aminolevulinic acid hydrochloride
Registration Number : 224MF10095
Registrant's Address : Heraeusstr. 12-14;63450 Hanau;Germany
Initial Date of Registration : 2012-04-27
Latest Date of Registration : 2024-06-18
Aminolevulinic acid hydrochloride
Registration Number : 229MF10010
Registrant's Address : 2-2 Nihonbashi Honcho 4-chome, Chuo-ku, Tokyo
Initial Date of Registration : 2017-01-18
Latest Date of Registration : 2017-01-18
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PharmaCompass offers a list of Aminolevulinic Acid HCl 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 Aminolevulinic Acid HCl manufacturer or Aminolevulinic Acid HCl supplier for your needs.
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PharmaCompass also assists you with knowing the Aminolevulinic Acid HCl API Price utilized in the formulation of products. Aminolevulinic Acid HCl API Price is not always fixed or binding as the Aminolevulinic Acid HCl Price is obtained through a variety of data sources. The Aminolevulinic Acid HCl Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 08340_FLUKA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 08340_FLUKA, including repackagers and relabelers. The FDA regulates 08340_FLUKA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 08340_FLUKA 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 08340_FLUKA supplier is an individual or a company that provides 08340_FLUKA active pharmaceutical ingredient (API) or 08340_FLUKA finished formulations upon request. The 08340_FLUKA suppliers may include 08340_FLUKA API manufacturers, exporters, distributors and traders.
click here to find a list of 08340_FLUKA 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 08340_FLUKA Drug Master File in Japan (08340_FLUKA JDMF) empowers 08340_FLUKA 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 08340_FLUKA JDMF during the approval evaluation for pharmaceutical products. At the time of 08340_FLUKA 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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