01 1BIOINDUSTRIA L.I.M. S.P.A. Novi Ligure IT
01 1Prazosin hydrochloride
01 1Italy
01 1Valid
Certificate Number : R1-CEP 2004-221 - Rev 03
Status : Valid
Issue Date : 2021-06-07
Type : Chemical
Substance Number : 856
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PharmaCompass offers a list of Prazosin Hydrochloride 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 Prazosin Hydrochloride manufacturer or Prazosin Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Prazosin Hydrochloride API Price utilized in the formulation of products. Prazosin Hydrochloride API Price is not always fixed or binding as the Prazosin Hydrochloride Price is obtained through a variety of data sources. The Prazosin Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Minipress Xl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Minipress Xl, including repackagers and relabelers. The FDA regulates Minipress Xl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Minipress Xl 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 Minipress Xl supplier is an individual or a company that provides Minipress Xl active pharmaceutical ingredient (API) or Minipress Xl finished formulations upon request. The Minipress Xl suppliers may include Minipress Xl API manufacturers, exporters, distributors and traders.
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A Minipress Xl CEP of the European Pharmacopoeia monograph is often referred to as a Minipress Xl Certificate of Suitability (COS). The purpose of a Minipress Xl CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Minipress Xl EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Minipress Xl to their clients by showing that a Minipress Xl CEP has been issued for it. The manufacturer submits a Minipress Xl CEP (COS) as part of the market authorization procedure, and it takes on the role of a Minipress Xl CEP holder for the record. Additionally, the data presented in the Minipress Xl CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Minipress Xl DMF.
A Minipress Xl CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Minipress Xl 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 Minipress Xl suppliers with CEP (COS) on PharmaCompass.
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