01 2APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
02 1CENTRIENT PHARMACEUTICALS NETHERLANDS B.V. Delft NL
01 1Oxacillin sodium monohydrate
02 1Oxacillin sodium monohydrate, Powder and compacted
03 1Oxacillin sodium monohydrate, Sterile
01 2India
02 1Netherlands
01 2Valid
02 1Withdrawn by Holder
Certificate Number : CEP 2007-349 - Rev 06
Status : Valid
Issue Date : 2023-11-30
Type : Chemical
Substance Number : 2260
Oxacillin Sodium Monohydrate, Sterile
Certificate Number : CEP 2007-363 - Rev 04
Status : Valid
Issue Date : 2023-11-30
Type : Chemical
Substance Number : 2260
Oxacillin Sodium Monohydrate, Powder And Compact...
Certificate Number : R1-CEP 2006-251 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2019-04-24
Type : Chemical
Substance Number : 2260
93
PharmaCompass offers a list of Oxacillin Sodium 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 Oxacillin Sodium manufacturer or Oxacillin Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Oxacillin Sodium API Price utilized in the formulation of products. Oxacillin Sodium API Price is not always fixed or binding as the Oxacillin Sodium Price is obtained through a variety of data sources. The Oxacillin Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Oxacillin Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxacillin Sodium, including repackagers and relabelers. The FDA regulates Oxacillin Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxacillin Sodium 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 Oxacillin Sodium supplier is an individual or a company that provides Oxacillin Sodium active pharmaceutical ingredient (API) or Oxacillin Sodium finished formulations upon request. The Oxacillin Sodium suppliers may include Oxacillin Sodium API manufacturers, exporters, distributors and traders.
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A Oxacillin Sodium CEP of the European Pharmacopoeia monograph is often referred to as a Oxacillin Sodium Certificate of Suitability (COS). The purpose of a Oxacillin Sodium CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Oxacillin Sodium EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Oxacillin Sodium to their clients by showing that a Oxacillin Sodium CEP has been issued for it. The manufacturer submits a Oxacillin Sodium CEP (COS) as part of the market authorization procedure, and it takes on the role of a Oxacillin Sodium CEP holder for the record. Additionally, the data presented in the Oxacillin Sodium CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Oxacillin Sodium DMF.
A Oxacillin Sodium CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Oxacillin Sodium CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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