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
Certificate Number : R1-CEP 2014-277 - Rev 00
Status : Valid
Issue Date : 2021-10-27
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
A Levocabastine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levocabastine, including repackagers and relabelers. The FDA regulates Levocabastine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levocabastine 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 Levocabastine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levocabastine supplier is an individual or a company that provides Levocabastine active pharmaceutical ingredient (API) or Levocabastine finished formulations upon request. The Levocabastine suppliers may include Levocabastine API manufacturers, exporters, distributors and traders.
click here to find a list of Levocabastine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Levocabastine CEP of the European Pharmacopoeia monograph is often referred to as a Levocabastine Certificate of Suitability (COS). The purpose of a Levocabastine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Levocabastine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Levocabastine to their clients by showing that a Levocabastine CEP has been issued for it. The manufacturer submits a Levocabastine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Levocabastine CEP holder for the record. Additionally, the data presented in the Levocabastine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Levocabastine DMF.
A Levocabastine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Levocabastine 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 Levocabastine suppliers with CEP (COS) on PharmaCompass.
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