01 1Becton, Dickinson and Company Sparks US
01 1Neomycin Assay Agar, (Antibiotic Medium 11, Product codes 210977 and 210980)
01 1U.S.A
01 1Withdrawn by Holder
Neomycin Assay Agar, (Antibiotic Medium 11, Prod...
Certificate Number : R0-CEP 2000-357 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2005-02-22
Type : TSE
Substance Number :
94
PharmaCompass offers a list of Neamine 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 Neamine manufacturer or Neamine supplier for your needs.
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PharmaCompass also assists you with knowing the Neamine API Price utilized in the formulation of products. Neamine API Price is not always fixed or binding as the Neamine Price is obtained through a variety of data sources. The Neamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Neamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neamine, including repackagers and relabelers. The FDA regulates Neamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neamine API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Neamine supplier is an individual or a company that provides Neamine active pharmaceutical ingredient (API) or Neamine finished formulations upon request. The Neamine suppliers may include Neamine API manufacturers, exporters, distributors and traders.
A Neamine CEP of the European Pharmacopoeia monograph is often referred to as a Neamine Certificate of Suitability (COS). The purpose of a Neamine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Neamine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Neamine to their clients by showing that a Neamine CEP has been issued for it. The manufacturer submits a Neamine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Neamine CEP holder for the record. Additionally, the data presented in the Neamine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Neamine DMF.
A Neamine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Neamine 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 Neamine suppliers with CEP (COS) on PharmaCompass.
