Inke S.A: APIs manufacturing plant.
01 1Inke, S.A. Castellbisbal ES
02 1EGIS Pharmaceuticals PLC Budapest HU
03 1SIEGFRIED LTD Zofingen CH
04 1Union Quimico Farmaceutica, S.A. (Uquifa S.A.) Barcelona ES
01 4Nitrendipine
01 1Hungary
02 2Spain
03 1Switzerland
01 3Valid
02 1Withdrawn by Holder
Inke S.A: APIs manufacturing plant.
Inke S.A: APIs manufacturing plant.
Certificate Number : R1-CEP 2000-132 - Rev 01
Status : Valid
Issue Date : 2012-06-20
Type : Chemical
Substance Number : 1246
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
Certificate Number : R0-CEP 2019-209 - Rev 00
Status : Valid
Issue Date : 2020-09-02
Type : Chemical
Substance Number : 1246
Certificate Number : R1-CEP 1999-041 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2009-10-28
Type : Chemical
Substance Number : 1246
Certificate Number : R1-CEP 2017-032 - Rev 00
Status : Valid
Issue Date : 2023-03-24
Type : Chemical
Substance Number : 1246
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PharmaCompass offers a list of Nitrendipine 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 Nitrendipine manufacturer or Nitrendipine supplier for your needs.
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PharmaCompass also assists you with knowing the Nitrendipine API Price utilized in the formulation of products. Nitrendipine API Price is not always fixed or binding as the Nitrendipine Price is obtained through a variety of data sources. The Nitrendipine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bayotensin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bayotensin, including repackagers and relabelers. The FDA regulates Bayotensin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bayotensin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Bayotensin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bayotensin supplier is an individual or a company that provides Bayotensin active pharmaceutical ingredient (API) or Bayotensin finished formulations upon request. The Bayotensin suppliers may include Bayotensin API manufacturers, exporters, distributors and traders.
click here to find a list of Bayotensin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Bayotensin CEP of the European Pharmacopoeia monograph is often referred to as a Bayotensin Certificate of Suitability (COS). The purpose of a Bayotensin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Bayotensin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Bayotensin to their clients by showing that a Bayotensin CEP has been issued for it. The manufacturer submits a Bayotensin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Bayotensin CEP holder for the record. Additionally, the data presented in the Bayotensin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Bayotensin DMF.
A Bayotensin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Bayotensin 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 Bayotensin suppliers with CEP (COS) on PharmaCompass.
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