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01 1PharmaZell (India) Private Limited
02 2PharmaZell (India)Private Limited
03 3MOEHS IBERICA S. L.
04 1Alfresa Fine Chemicals Co., Ltd.
05 1Bretagne Chimie Fine
06 1DaeBong LS CO. ,LTD
07 2Ilshin Chemical Co. , Ltd.
08 1Taenaka Mining Co., Ltd.
01 1"Japan-station" L- carboxymethyl cysteine (production only)
02 1CARBOCISTEINE
03 2Japanese Pharmacopoeia carboxymethyl cysteine (production only)
04 4L- carbocisteine
05 4L-Carbocisteine
01 1France
02 3Germany
03 2Japan
04 3South Korea
05 3Spain
Registration Number : 227MF10185
Registrant's Address : Plot No. B5 & B6, MEPZ, Tambaram, Chennai 600 045, India
Initial Date of Registration : 2015-07-13
Latest Date of Registration : 2021-07-16
Registration Number : 302MF10142
Registrant's Address : Cesar Martinell I brunet 12A, Poligono Rubi Sur, Rubi (Barcelona), Spain
Initial Date of Registration : 2020-11-30
Latest Date of Registration : 2020-11-30
"JP" L-Carbocisteine (for manufacturing purposes only)
Registration Number : 218MF10008
Registrant's Address : Plot No. B5 & B6, MEPZ, Tambaram, Chennai 600 045, India
Initial Date of Registration : 2006-01-27
Latest Date of Registration : 2008-02-25
Registration Number : 225MF10208
Registrant's Address : Plot No. B5 & B6, MEPZ, Tambaram, Chennai 600 045, India
Initial Date of Registration : 2013-11-14
Latest Date of Registration : 2021-07-16
Registration Number : 227MF10075
Registrant's Address : Cesar Martinell i Brunet 12A, Poligono Rubi Sur, Rubi (Barcelona), Spain
Initial Date of Registration : 2015-03-12
Latest Date of Registration : 2018-07-09
Registration Number : 217MF10568
Registrant's Address : Cesar Martinell i Brunet 12A, Poligono Rubi Sur, Rubi (Barcelona), Spain
Initial Date of Registration : 2005-09-09
Latest Date of Registration : 2018-06-26
Registration Number : 301MF10093
Registrant's Address : 1-10-1 Mukaihama, Akita City, Akita Prefecture
Initial Date of Registration : 2019-11-15
Latest Date of Registration : 2019-11-15
Registration Number : 231MF10065
Registrant's Address : Boisel 56140 PLEUCADEUC FRANCE
Initial Date of Registration : 2019-03-05
Latest Date of Registration : 2019-03-05
Registration Number : 227MF10241
Registrant's Address : 123, Neungheodae-ro 649 beongil, Namdong-gu, Incheon-city, KOREA
Initial Date of Registration : 2015-09-29
Latest Date of Registration : 2015-09-29
Registration Number : 301MF10092
Registrant's Address : 1042, YANGSAN-DAERO, YANGSAN-SI, GYEONGSANGNAM-DO, KOREA
Initial Date of Registration : 2019-11-15
Latest Date of Registration : 2019-11-15
A Carbocisteine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Carbocisteine, including repackagers and relabelers. The FDA regulates Carbocisteine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Carbocisteine 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 Carbocisteine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Carbocisteine supplier is an individual or a company that provides Carbocisteine active pharmaceutical ingredient (API) or Carbocisteine finished formulations upon request. The Carbocisteine suppliers may include Carbocisteine API manufacturers, exporters, distributors and traders.
click here to find a list of Carbocisteine 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 Carbocisteine Drug Master File in Japan (Carbocisteine JDMF) empowers Carbocisteine 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 Carbocisteine JDMF during the approval evaluation for pharmaceutical products. At the time of Carbocisteine 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 Carbocisteine suppliers with JDMF on PharmaCompass.
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