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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A levophta manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of levophta, including repackagers and relabelers. The FDA regulates levophta manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. levophta 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 levophta supplier is an individual or a company that provides levophta active pharmaceutical ingredient (API) or levophta finished formulations upon request. The levophta suppliers may include levophta API manufacturers, exporters, distributors and traders.
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A levophta CEP of the European Pharmacopoeia monograph is often referred to as a levophta Certificate of Suitability (COS). The purpose of a levophta CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of levophta EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of levophta to their clients by showing that a levophta CEP has been issued for it. The manufacturer submits a levophta CEP (COS) as part of the market authorization procedure, and it takes on the role of a levophta CEP holder for the record. Additionally, the data presented in the levophta CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the levophta DMF.
A levophta CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. levophta CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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