01 2DR. PAUL LOHMANN GMBH & CO. KGAA Emmerthal DE
01 1Ferrous sulfate heptahydrate
02 1Ferrous sulfate, dried, Powder, milled powder, micronised powder
01 2Germany
01 2Valid
Ferrous Sulfate, Dried, Powder, Milled Powder, M...
Certificate Number : R1-CEP 2007-368 - Rev 04
Status : Valid
Issue Date : 2022-01-28
Type : Chemical
Substance Number : 2340
Certificate Number : R1-CEP 2007-369 - Rev 03
Status : Valid
Issue Date : 2022-02-01
Type : Chemical
Substance Number : 83
81
PharmaCompass offers a list of Ferrous Sulfate 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 Sulfate manufacturer or Ferrous Sulfate supplier for your needs.
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PharmaCompass also assists you with knowing the Ferrous Sulfate API Price utilized in the formulation of products. Ferrous Sulfate API Price is not always fixed or binding as the Ferrous Sulfate Price is obtained through a variety of data sources. The Ferrous Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sorbifer durules manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sorbifer durules, including repackagers and relabelers. The FDA regulates Sorbifer durules manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sorbifer durules 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 Sorbifer durules supplier is an individual or a company that provides Sorbifer durules active pharmaceutical ingredient (API) or Sorbifer durules finished formulations upon request. The Sorbifer durules suppliers may include Sorbifer durules API manufacturers, exporters, distributors and traders.
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A Sorbifer durules CEP of the European Pharmacopoeia monograph is often referred to as a Sorbifer durules Certificate of Suitability (COS). The purpose of a Sorbifer durules CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Sorbifer durules EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Sorbifer durules to their clients by showing that a Sorbifer durules CEP has been issued for it. The manufacturer submits a Sorbifer durules CEP (COS) as part of the market authorization procedure, and it takes on the role of a Sorbifer durules CEP holder for the record. Additionally, the data presented in the Sorbifer durules CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Sorbifer durules DMF.
A Sorbifer durules CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Sorbifer durules 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 Sorbifer durules suppliers with CEP (COS) on PharmaCompass.
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