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01 1Nippon Protein Co., Ltd.
02 1Nippon Rika Pharmaceuticals Co., Ltd.
03 2Taenaka Mining Co., Ltd.
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01 1Japanese Pharmacopoeia L- cysteine
02 1Japanese Pharmacopoeia L- cystine (production only)
03 2Outsiders regulations L- cystine (production only)
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01 4Japan
Japanese Pharmacopoeia L-Cysteine
Registration Number : 219MF10338
Registrant's Address : 2-2 Nihonbashi Honcho 4-chome, Chuo-ku, Tokyo
Initial Date of Registration : 2007-11-21
Latest Date of Registration : 2007-11-21
Extra-official regulation L-cystine (for manufacturing only)
Registration Number : 218MF11012
Registrant's Address : 575 Shimada-cho, Ashikaga City, Tochigi Prefecture
Initial Date of Registration : 2006-12-18
Latest Date of Registration : 2006-12-18
Extra-official regulation L-cystine (for manufacturing only)
Registration Number : 217MF10284
Registrant's Address : 452 Oshiba, Mobara City, Chiba Prefecture
Initial Date of Registration : 2005-06-20
Latest Date of Registration : 2007-07-26
Japanese Pharmacopoeia L-Cystine (for manufacturing only)
Registration Number : 225MF10115
Registrant's Address : 452 Oshiba, Mobara City, Chiba Prefecture
Initial Date of Registration : 2013-06-07
Latest Date of Registration : 2013-06-07
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PharmaCompass offers a list of Cystine 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 Cystine manufacturer or Cystine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cystine manufacturer or Cystine supplier.
PharmaCompass also assists you with knowing the Cystine API Price utilized in the formulation of products. Cystine API Price is not always fixed or binding as the Cystine Price is obtained through a variety of data sources. The Cystine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ACETYLCYSTEINE IMPURITY A (L-CYSTINE) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ACETYLCYSTEINE IMPURITY A (L-CYSTINE), including repackagers and relabelers. The FDA regulates ACETYLCYSTEINE IMPURITY A (L-CYSTINE) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ACETYLCYSTEINE IMPURITY A (L-CYSTINE) 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 ACETYLCYSTEINE IMPURITY A (L-CYSTINE) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ACETYLCYSTEINE IMPURITY A (L-CYSTINE) supplier is an individual or a company that provides ACETYLCYSTEINE IMPURITY A (L-CYSTINE) active pharmaceutical ingredient (API) or ACETYLCYSTEINE IMPURITY A (L-CYSTINE) finished formulations upon request. The ACETYLCYSTEINE IMPURITY A (L-CYSTINE) suppliers may include ACETYLCYSTEINE IMPURITY A (L-CYSTINE) API manufacturers, exporters, distributors and traders.
click here to find a list of ACETYLCYSTEINE IMPURITY A (L-CYSTINE) 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 ACETYLCYSTEINE IMPURITY A (L-CYSTINE) Drug Master File in Japan (ACETYLCYSTEINE IMPURITY A (L-CYSTINE) JDMF) empowers ACETYLCYSTEINE IMPURITY A (L-CYSTINE) 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 ACETYLCYSTEINE IMPURITY A (L-CYSTINE) JDMF during the approval evaluation for pharmaceutical products. At the time of ACETYLCYSTEINE IMPURITY A (L-CYSTINE) 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 ACETYLCYSTEINE IMPURITY A (L-CYSTINE) suppliers with JDMF on PharmaCompass.
We have 3 companies offering ACETYLCYSTEINE IMPURITY A (L-CYSTINE)
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