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01 1Boehringer Ingelheim Pharma GmbH & Co. KG Ingelheim Am Rhein DE
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01 1Brotizolam, Micronised
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01 1Germany
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01 1Valid
Certificate Number : R1-CEP 2008-063 - Rev 00
Status : Valid
Issue Date : 2014-10-31
Type : Chemical
Substance Number : 2197
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PharmaCompass offers a list of Brotizolam 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 Brotizolam manufacturer or Brotizolam supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Brotizolam manufacturer or Brotizolam supplier.
PharmaCompass also assists you with knowing the Brotizolam API Price utilized in the formulation of products. Brotizolam API Price is not always fixed or binding as the Brotizolam Price is obtained through a variety of data sources. The Brotizolam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lendormin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lendormin, including repackagers and relabelers. The FDA regulates Lendormin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lendormin 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 Lendormin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lendormin supplier is an individual or a company that provides Lendormin active pharmaceutical ingredient (API) or Lendormin finished formulations upon request. The Lendormin suppliers may include Lendormin API manufacturers, exporters, distributors and traders.
click here to find a list of Lendormin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lendormin CEP of the European Pharmacopoeia monograph is often referred to as a Lendormin Certificate of Suitability (COS). The purpose of a Lendormin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Lendormin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Lendormin to their clients by showing that a Lendormin CEP has been issued for it. The manufacturer submits a Lendormin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Lendormin CEP holder for the record. Additionally, the data presented in the Lendormin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Lendormin DMF.
A Lendormin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Lendormin 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 Lendormin suppliers with CEP (COS) on PharmaCompass.
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