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01 1DR. PAUL LOHMANN GMBH & CO. KGAA Emmerthal DE
02 1FERROPHARMA CHEMICALS LTD. Dóc HU
03 1POLYDRUG LABORATORIES PVT. LTD. Mumbai IN
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01 3Ferrous fumarate
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01 1Germany
02 1India
03 1Indonesia
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01 2Valid
02 1Withdrawn by EDQM Failure to CEP procedure
Certificate Number : CEP 2004-232 - Rev 04
Status : Valid
Issue Date : 2025-01-21
Type : Chemical
Substance Number : 902
Certificate Number : R1-CEP 2012-400 - Rev 00
Status : Valid
Issue Date : 2020-02-19
Type : Chemical
Substance Number : 902
Certificate Number : R0-CEP 2010-147 - Rev 00
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2012-02-22
Type : Chemical
Substance Number : 902
22
PharmaCompass offers a list of Ferrous Fumarate 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 Ferrous Fumarate manufacturer or Ferrous Fumarate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ferrous Fumarate manufacturer or Ferrous Fumarate supplier.
PharmaCompass also assists you with knowing the Ferrous Fumarate API Price utilized in the formulation of products. Ferrous Fumarate API Price is not always fixed or binding as the Ferrous Fumarate Price is obtained through a variety of data sources. The Ferrous Fumarate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A LO-BLISOVI FE-2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LO-BLISOVI FE-2, including repackagers and relabelers. The FDA regulates LO-BLISOVI FE-2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LO-BLISOVI FE-2 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 LO-BLISOVI FE-2 supplier is an individual or a company that provides LO-BLISOVI FE-2 active pharmaceutical ingredient (API) or LO-BLISOVI FE-2 finished formulations upon request. The LO-BLISOVI FE-2 suppliers may include LO-BLISOVI FE-2 API manufacturers, exporters, distributors and traders.
click here to find a list of LO-BLISOVI FE-2 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A LO-BLISOVI FE-2 CEP of the European Pharmacopoeia monograph is often referred to as a LO-BLISOVI FE-2 Certificate of Suitability (COS). The purpose of a LO-BLISOVI FE-2 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of LO-BLISOVI FE-2 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of LO-BLISOVI FE-2 to their clients by showing that a LO-BLISOVI FE-2 CEP has been issued for it. The manufacturer submits a LO-BLISOVI FE-2 CEP (COS) as part of the market authorization procedure, and it takes on the role of a LO-BLISOVI FE-2 CEP holder for the record. Additionally, the data presented in the LO-BLISOVI FE-2 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the LO-BLISOVI FE-2 DMF.
A LO-BLISOVI FE-2 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. LO-BLISOVI FE-2 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 LO-BLISOVI FE-2 suppliers with CEP (COS) on PharmaCompass.
We have 3 companies offering LO-BLISOVI FE-2
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