AMI Lifesciences is Driven by Chemistry. Powered by People.
01 1AMI LIFESCIENCES PRIVATE LIMITED Karakhadi IN
02 1ARCHIMICA S.P.A Lodi IT
03 1EUTICALS S.P.A. Casaletto Lodigiano IT
04 1ICROM S.R.L. Concorezzo IT
05 1Interquim S.A. DE C.V. Estado De Mexico MX
01 5Diacerein
01 1India
02 3Italy
03 1Mexico
01 1Expired
02 4Valid
AMI Lifesciences is Driven by Chemistry. Powered by People.
AMI Lifesciences is Driven by Chemistry. Powered by People.
Certificate Number : CEP 2015-173 - Rev 03
Status : Valid
Issue Date : 2024-12-03
Type : Chemical
Substance Number : 2409
Certificate Number : R1-CEP 2014-247 - Rev 00
Status : Valid
Issue Date : 2021-06-24
Type : Chemical
Substance Number : 2409
Certificate Number : R0-CEP 2014-248 - Rev 00
Status : Expired
Issue Date : 2016-07-21
Type : Chemical
Substance Number : 2409
Certificate Number : CEP 2017-148 - Rev 03
Status : Valid
Issue Date : 2024-03-26
Type : Chemical
Substance Number : 2409
Certificate Number : R0-CEP 2021-483 - Rev 00
Status : Valid
Issue Date : 2023-05-30
Type : Chemical
Substance Number : 2409
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PharmaCompass offers a list of Diacerein 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 Diacerein manufacturer or Diacerein supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Diacerein manufacturer or Diacerein supplier.
PharmaCompass also assists you with knowing the Diacerein API Price utilized in the formulation of products. Diacerein API Price is not always fixed or binding as the Diacerein Price is obtained through a variety of data sources. The Diacerein Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Artrodar manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Artrodar, including repackagers and relabelers. The FDA regulates Artrodar manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Artrodar 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 Artrodar manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Artrodar supplier is an individual or a company that provides Artrodar active pharmaceutical ingredient (API) or Artrodar finished formulations upon request. The Artrodar suppliers may include Artrodar API manufacturers, exporters, distributors and traders.
click here to find a list of Artrodar suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Artrodar CEP of the European Pharmacopoeia monograph is often referred to as a Artrodar Certificate of Suitability (COS). The purpose of a Artrodar CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Artrodar EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Artrodar to their clients by showing that a Artrodar CEP has been issued for it. The manufacturer submits a Artrodar CEP (COS) as part of the market authorization procedure, and it takes on the role of a Artrodar CEP holder for the record. Additionally, the data presented in the Artrodar CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Artrodar DMF.
A Artrodar CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Artrodar 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 Artrodar suppliers with CEP (COS) on PharmaCompass.
We have 4 companies offering Artrodar
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