01 1KRKA, d.d., Novo mesto Novo mesto SI
02 1North China Pharmaceutical Huasheng Co., Ltd. Shijiazhuang CN
03 3XELLIA PHARMACEUTICALS APS Copenhagen S DK
01 1Bacitracin
02 2Bacitracin zinc
03 1Bacitracin, Micronised, non-micronised
04 1Bacitracin, Sterile
01 1China
02 3Denmark
03 1Slovenia
01 4Valid
02 1Withdrawn by Holder
Certificate Number : R0-CEP 2006-052 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2008-11-07
Type : Chemical
Substance Number : 466
Certificate Number : CEP 2017-293 - Rev 01
Status : Valid
Issue Date : 2024-09-18
Type : Chemical
Substance Number : 465
Bacitracin, Micronised, Non-micronised
Certificate Number : CEP 2002-226 - Rev 08
Status : Valid
Issue Date : 2024-08-22
Type : Chemical
Substance Number : 465
Certificate Number : R1-CEP 2002-103 - Rev 10
Status : Valid
Issue Date : 2022-08-18
Type : Chemical
Substance Number : 466
Certificate Number : R1-CEP 2002-224 - Rev 08
Status : Valid
Issue Date : 2018-02-07
Type : Chemical
Substance Number : 465
10
PharmaCompass offers a list of Bacitracin Zinc 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 Bacitracin Zinc manufacturer or Bacitracin Zinc supplier for your needs.
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PharmaCompass also assists you with knowing the Bacitracin Zinc API Price utilized in the formulation of products. Bacitracin Zinc API Price is not always fixed or binding as the Bacitracin Zinc Price is obtained through a variety of data sources. The Bacitracin Zinc Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ZIBA-RX manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ZIBA-RX, including repackagers and relabelers. The FDA regulates ZIBA-RX manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ZIBA-RX 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 ZIBA-RX supplier is an individual or a company that provides ZIBA-RX active pharmaceutical ingredient (API) or ZIBA-RX finished formulations upon request. The ZIBA-RX suppliers may include ZIBA-RX API manufacturers, exporters, distributors and traders.
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A ZIBA-RX CEP of the European Pharmacopoeia monograph is often referred to as a ZIBA-RX Certificate of Suitability (COS). The purpose of a ZIBA-RX CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of ZIBA-RX EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of ZIBA-RX to their clients by showing that a ZIBA-RX CEP has been issued for it. The manufacturer submits a ZIBA-RX CEP (COS) as part of the market authorization procedure, and it takes on the role of a ZIBA-RX CEP holder for the record. Additionally, the data presented in the ZIBA-RX CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the ZIBA-RX DMF.
A ZIBA-RX CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. ZIBA-RX 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 ZIBA-RX suppliers with CEP (COS) on PharmaCompass.
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