01 2DR. PAUL LOHMANN GMBH & CO. KGAA Emmerthal DE
02 1Global Calcium Private Limited Hosur IN
03 1JUNGBUNZLAUER LADENBURG GMBH Ladenburg DE
01 2Magnesium citrate
02 1Magnesium citrate nonahydrate, Powder, micronised powder, granules
03 1Magnesium citrate, Powdered or granulated
01 2Germany
02 1India
03 1Switzerland
01 3Valid
02 1Withdrawn by EDQM Failure to CEP procedure
Magnesium Citrate Nonahydrate, Powder, Micronise...
Certificate Number : CEP 2011-036 - Rev 03
Status : Valid
Issue Date : 2025-01-03
Type : Chemical
Substance Number : 2402
Magnesium Citrate, Powdered Or Granulated
Certificate Number : R1-CEP 2009-017 - Rev 03
Status : Valid
Issue Date : 2021-10-29
Type : Chemical
Substance Number : 2339
Certificate Number : R0-CEP 2009-151 - Rev 00
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2010-10-26
Type : Chemical
Substance Number : 2339
Certificate Number : R1-CEP 2015-129 - Rev 01
Status : Valid
Issue Date : 2022-10-19
Type : Chemical
Substance Number : 2339
11
PharmaCompass offers a list of Magnesium Citrate 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 Magnesium Citrate manufacturer or Magnesium Citrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Magnesium Citrate manufacturer or Magnesium Citrate supplier.
PharmaCompass also assists you with knowing the Magnesium Citrate API Price utilized in the formulation of products. Magnesium Citrate API Price is not always fixed or binding as the Magnesium Citrate Price is obtained through a variety of data sources. The Magnesium Citrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 3344-18-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 3344-18-1, including repackagers and relabelers. The FDA regulates 3344-18-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 3344-18-1 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 3344-18-1 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 3344-18-1 supplier is an individual or a company that provides 3344-18-1 active pharmaceutical ingredient (API) or 3344-18-1 finished formulations upon request. The 3344-18-1 suppliers may include 3344-18-1 API manufacturers, exporters, distributors and traders.
click here to find a list of 3344-18-1 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 3344-18-1 CEP of the European Pharmacopoeia monograph is often referred to as a 3344-18-1 Certificate of Suitability (COS). The purpose of a 3344-18-1 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 3344-18-1 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 3344-18-1 to their clients by showing that a 3344-18-1 CEP has been issued for it. The manufacturer submits a 3344-18-1 CEP (COS) as part of the market authorization procedure, and it takes on the role of a 3344-18-1 CEP holder for the record. Additionally, the data presented in the 3344-18-1 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 3344-18-1 DMF.
A 3344-18-1 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 3344-18-1 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 3344-18-1 suppliers with CEP (COS) on PharmaCompass.
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