01 1Janssen Pharmaceutica NV
02 3Katsura Chemical Co., Ltd.
01 1Levocabastine Hydrochloride-K
02 2Levocabastine hydrochloride
03 1Levocabastine hydrochloride-S
01 3Japan
02 1U.S.A
Registration Number : 228MF10206
Registrant's Address : Turnhoutseweg 30 B-2340 Beerse Belgium
Initial Date of Registration : 2016-11-02
Latest Date of Registration : 2016-11-02
Registration Number : 230MF10168
Registrant's Address : 4-15-19 Hibarigaoka, Zama City, Kanagawa Prefecture
Initial Date of Registration : 2018-12-19
Latest Date of Registration : 2018-12-19
Registration Number : 218MF10995
Registrant's Address : 4-15-19 Hibarigaoka, Zama City, Kanagawa Prefecture
Initial Date of Registration : 2006-12-18
Latest Date of Registration : 2008-11-25
Registration Number : 306MF10125
Registrant's Address : 4-15-19 Hibarigaoka, Zama City, Kanagawa Prefecture
Initial Date of Registration : 2024-09-11
Latest Date of Registration : 2024-09-11
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PharmaCompass offers a list of Levocabastine 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 Levocabastine manufacturer or Levocabastine supplier for your needs.
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PharmaCompass also assists you with knowing the Levocabastine API Price utilized in the formulation of products. Levocabastine API Price is not always fixed or binding as the Levocabastine Price is obtained through a variety of data sources. The Levocabastine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A livostin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of livostin, including repackagers and relabelers. The FDA regulates livostin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. livostin 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 livostin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A livostin supplier is an individual or a company that provides livostin active pharmaceutical ingredient (API) or livostin finished formulations upon request. The livostin suppliers may include livostin API manufacturers, exporters, distributors and traders.
click here to find a list of livostin 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 livostin Drug Master File in Japan (livostin JDMF) empowers livostin 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 livostin JDMF during the approval evaluation for pharmaceutical products. At the time of livostin 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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