01 1CURIA SPAIN S.A.U. Boecillo ES
02 1JANSSEN PHARMACEUTICA NV Beerse BE
03 2KATSURA CHEMICAL CO., LTD. Zama JP
01 3Levocabastine hydrochloride
02 1Levocabastine hydrochloride, Process Part 2
01 1Belgium
02 2Japan
03 1U.S.A
01 4Valid
Certificate Number : R1-CEP 2012-002 - Rev 04
Status : Valid
Issue Date : 2021-11-16
Type : Chemical
Substance Number : 1484
Certificate Number : R1-CEP 2002-147 - Rev 03
Status : Valid
Issue Date : 2020-12-09
Type : Chemical
Substance Number : 1484
Levocabastine Hydrochloride, Process Part 2
Certificate Number : CEP 2018-217 - Rev 01
Status : Valid
Issue Date : 2024-09-02
Type : Chemical
Substance Number : 1484
Certificate Number : R1-CEP 2014-277 - Rev 00
Status : Valid
Issue Date : 2021-10-27
Type : Chemical
Substance Number : 1484
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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 livocab manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of livocab, including repackagers and relabelers. The FDA regulates livocab manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. livocab API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A livocab supplier is an individual or a company that provides livocab active pharmaceutical ingredient (API) or livocab finished formulations upon request. The livocab suppliers may include livocab API manufacturers, exporters, distributors and traders.
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A livocab CEP of the European Pharmacopoeia monograph is often referred to as a livocab Certificate of Suitability (COS). The purpose of a livocab CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of livocab EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of livocab to their clients by showing that a livocab CEP has been issued for it. The manufacturer submits a livocab CEP (COS) as part of the market authorization procedure, and it takes on the role of a livocab CEP holder for the record. Additionally, the data presented in the livocab CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the livocab DMF.
A livocab CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. livocab CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of livocab suppliers with CEP (COS) on PharmaCompass.
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