01 2CHENGDA PHARMACEUTICALS CO. , LTD.
02 2Kongo Chemical Co., Ltd.
03 1Liaoning Koncepnutra Co. , Ltd.
04 1Northeast Pharmaceutical Group Co. , Ltd.
01 1Carnitine chloride (production only)
02 1Levocarnine
03 2Levocarnitine
04 1Levocarnitine chloride
05 1Levocarnitine chloride "Congo"
01 4China
02 2Japan
Registration Number : 301MF10030
Registrant's Address : No. 36, Huanghe Road, Huimin Subdistrict, Jiashan, Jiaxing, Zhejiang, 314100, China
Initial Date of Registration : 2019-07-10
Latest Date of Registration : 2019-07-10
Registration Number : 225MF10026
Registrant's Address : No. 5, Hengshan Road, United Development Zone, Jia Shan, Zhejiang, China
Initial Date of Registration : 2013-02-13
Latest Date of Registration : 2013-02-13
Levocarnitine chloride "Congo"
Registration Number : 221MF10004
Registrant's Address : 3 Himata, Toyama City, Toyama Prefecture
Initial Date of Registration : 2009-01-13
Latest Date of Registration : 2009-01-13
Carnitine chloride (for manufacturing only)
Registration Number : 217MF11192
Registrant's Address : 3 Himata, Toyama City, Toyama Prefecture
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2010-03-09
Registration Number : 303MF10023
Registrant's Address : No. 100 Xianghuai Road, Benxi Economic Development Zone, Liaoning, China
Initial Date of Registration : 2021-02-01
Latest Date of Registration : 2021-11-17
Registration Number : 303MF10012
Registrant's Address : No. 8, Kunminghu Street, Economic & Technology Development District, Shenyang, China
Initial Date of Registration : 2021-01-26
Latest Date of Registration : 2021-01-26
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PharmaCompass offers a list of Levocarnitine 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 Levocarnitine manufacturer or Levocarnitine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Levocarnitine manufacturer or Levocarnitine supplier.
PharmaCompass also assists you with knowing the Levocarnitine API Price utilized in the formulation of products. Levocarnitine API Price is not always fixed or binding as the Levocarnitine Price is obtained through a variety of data sources. The Levocarnitine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CS-2495 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CS-2495, including repackagers and relabelers. The FDA regulates CS-2495 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CS-2495 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 CS-2495 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CS-2495 supplier is an individual or a company that provides CS-2495 active pharmaceutical ingredient (API) or CS-2495 finished formulations upon request. The CS-2495 suppliers may include CS-2495 API manufacturers, exporters, distributors and traders.
click here to find a list of CS-2495 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 CS-2495 Drug Master File in Japan (CS-2495 JDMF) empowers CS-2495 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 CS-2495 JDMF during the approval evaluation for pharmaceutical products. At the time of CS-2495 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 CS-2495 suppliers with JDMF on PharmaCompass.
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