01 1INDOCO REMEDIES LIMITED Mumbai IN
01 1Dicycloverine Hydrochloride
01 1India
01 1Valid
Certificate Number : CEP 2008-281 - Rev 06
Status : Valid
Issue Date : 2024-01-17
Type : Chemical
Substance Number : 1197
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PharmaCompass offers a list of Dicyclomine 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 Dicyclomine Hydrochloride manufacturer or Dicyclomine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dicyclomine Hydrochloride manufacturer or Dicyclomine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Dicyclomine Hydrochloride API Price utilized in the formulation of products. Dicyclomine Hydrochloride API Price is not always fixed or binding as the Dicyclomine Hydrochloride Price is obtained through a variety of data sources. The Dicyclomine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bentylol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bentylol, including repackagers and relabelers. The FDA regulates Bentylol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bentylol 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 Bentylol supplier is an individual or a company that provides Bentylol active pharmaceutical ingredient (API) or Bentylol finished formulations upon request. The Bentylol suppliers may include Bentylol API manufacturers, exporters, distributors and traders.
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A Bentylol CEP of the European Pharmacopoeia monograph is often referred to as a Bentylol Certificate of Suitability (COS). The purpose of a Bentylol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Bentylol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Bentylol to their clients by showing that a Bentylol CEP has been issued for it. The manufacturer submits a Bentylol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Bentylol CEP holder for the record. Additionally, the data presented in the Bentylol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Bentylol DMF.
A Bentylol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Bentylol 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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