IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
01 1PHARMASYNTHESE Saint Pierre Les Elbeuf FR
02 1OLON S.P.A. Rodano IT
03 1OPTIMUS DRUGS PRIVATE LIMITED Hyderabad IN
04 2SIEGFRIED LTD. Zofingen CH
05 1ZHEJIANG HISOAR PHARMACEUTICAL CO., LTD. Taizhou CN
01 5Amorolfine hydrochloride
02 1Amorolfine hydrochloride, Nantong site
01 1China
02 1France
03 1India
04 1Italy
05 2Switzerland
01 6Valid
IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
Certificate Number : CEP 2016-312 - Rev 01
Status : Valid
Issue Date : 2024-10-29
Type : Chemical
Substance Number : 2756
Certificate Number : CEP 2016-071 - Rev 01
Status : Valid
Issue Date : 2024-09-11
Type : Chemical
Substance Number : 2756
Certificate Number : R0-CEP 2021-046 - Rev 00
Status : Valid
Issue Date : 2023-05-02
Type : Chemical
Substance Number : 2756
Amorolfine Hydrochloride, Nantong Site
Certificate Number : R1-CEP 2017-251 - Rev 00
Status : Valid
Issue Date : 2023-01-11
Type : Chemical
Substance Number : 2756
Certificate Number : R1-CEP 2016-094 - Rev 00
Status : Valid
Issue Date : 2022-05-24
Type : Chemical
Substance Number : 2756
Certificate Number : R1-CEP 2017-091 - Rev 00
Status : Valid
Issue Date : 2023-02-02
Type : Chemical
Substance Number : 2756
A Amorolfine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Amorolfine Hydrochloride, including repackagers and relabelers. The FDA regulates Amorolfine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Amorolfine Hydrochloride 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 Amorolfine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Amorolfine Hydrochloride supplier is an individual or a company that provides Amorolfine Hydrochloride active pharmaceutical ingredient (API) or Amorolfine Hydrochloride finished formulations upon request. The Amorolfine Hydrochloride suppliers may include Amorolfine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Amorolfine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Amorolfine Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Amorolfine Hydrochloride Certificate of Suitability (COS). The purpose of a Amorolfine Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Amorolfine Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Amorolfine Hydrochloride to their clients by showing that a Amorolfine Hydrochloride CEP has been issued for it. The manufacturer submits a Amorolfine Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Amorolfine Hydrochloride CEP holder for the record. Additionally, the data presented in the Amorolfine Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Amorolfine Hydrochloride DMF.
A Amorolfine Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Amorolfine Hydrochloride 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 Amorolfine Hydrochloride suppliers with CEP (COS) on PharmaCompass.
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