Axplora is your partner of choice for complex APIs.
01 1PharmaZell GmbH
02 3Nippon Protein Co., Ltd.
03 2Nippon Rika Pharmaceuticals Co., Ltd.
01 1Acetylcysteine
02 1Japanese Pharmacopoeia-acetyl-cysteine
03 1Japanese Pharmacopoeia-acetylcysteine "production-only"
04 1Outsiders regulations acetylcysteine
05 2Outsiders regulations acetylcysteine (production only)
01 1Germany
02 5Japan
Axplora is your partner of choice for complex APIs.
Registration Number : 219MF10377
Registrant's Address : ROSENHEIMER STR. 43, D-83064 RAUBLING, GERMARY
Initial Date of Registration : 2007-12-19
Latest Date of Registration : 2007-12-19
Japanese Pharmacopoeia Acetylcysteine "For manufacturing only"
Registration Number : 224MF10007
Registrant's Address : 575 Shimada-cho, Ashikaga City, Tochigi Prefecture
Initial Date of Registration : 2012-01-18
Latest Date of Registration : 2012-01-18
Acetylcysteine (for manufacturing only)
Registration Number : 220MF10106
Registrant's Address : 575 Shimada-cho, Ashikaga City, Tochigi Prefecture
Initial Date of Registration : 2008-04-11
Latest Date of Registration : 2008-04-11
Acetylcysteine (for manufacturing only)
Registration Number : 218MF10577
Registrant's Address : 575 Shimada-cho, Ashikaga City, Tochigi Prefecture
Initial Date of Registration : 2006-06-15
Latest Date of Registration : 2006-06-15
Japanese Pharmacopoeia Acetylcysteine
Registration Number : 224MF10025
Registrant's Address : 2-2 Nihonbashi Honcho 4-chome, Chuo-ku, Tokyo
Initial Date of Registration : 2012-02-01
Latest Date of Registration : 2012-02-01
Registration Number : 217MF10061
Registrant's Address : 4-2-2 Nihonbashi Honcho, Chuo Ward, Tokyo
Initial Date of Registration : 2005-05-20
Latest Date of Registration : 2006-05-18
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PharmaCompass offers a list of Acetylcysteine 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 Acetylcysteine manufacturer or Acetylcysteine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Acetylcysteine manufacturer or Acetylcysteine supplier.
PharmaCompass also assists you with knowing the Acetylcysteine API Price utilized in the formulation of products. Acetylcysteine API Price is not always fixed or binding as the Acetylcysteine Price is obtained through a variety of data sources. The Acetylcysteine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Flumil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flumil, including repackagers and relabelers. The FDA regulates Flumil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flumil 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 Flumil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Flumil supplier is an individual or a company that provides Flumil active pharmaceutical ingredient (API) or Flumil finished formulations upon request. The Flumil suppliers may include Flumil API manufacturers, exporters, distributors and traders.
click here to find a list of Flumil 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 Flumil Drug Master File in Japan (Flumil JDMF) empowers Flumil 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 Flumil JDMF during the approval evaluation for pharmaceutical products. At the time of Flumil 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 Flumil suppliers with JDMF on PharmaCompass.
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