01 2Bidachem S.p.A. Fornovo San Giovanni IT
02 1DISHMAN CARBOGEN AMCIS LIMITED Ahmedabad IN
03 1Erregierre S.p.A. San Paolo D'Argon IT
04 1KREATIVE ORGANICS PRIVATE LIMITED Hyderabad IN
01 3Bisacodyl
02 1Bisacodyl, Micronised
03 1Bisacodyl, Powder
01 1India
02 3Italy
03 1Switzerland
01 5Valid
Certificate Number : R1-CEP 2004-037 - Rev 00
Status : Valid
Issue Date : 2010-01-07
Type : Chemical
Substance Number : 595
Certificate Number : R1-CEP 2003-067 - Rev 00
Status : Valid
Issue Date : 2010-01-07
Type : Chemical
Substance Number : 595
Certificate Number : CEP 2007-163 - Rev 04
Status : Valid
Issue Date : 2024-07-15
Type : Chemical
Substance Number : 595
Certificate Number : R0-CEP 2020-233 - Rev 00
Status : Valid
Issue Date : 2022-03-01
Type : Chemical
Substance Number : 595
Certificate Number : CEP 2019-247 - Rev 01
Status : Valid
Issue Date : 2024-09-18
Type : Chemical
Substance Number : 595
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PharmaCompass offers a list of Bisacodyl 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 Bisacodyl manufacturer or Bisacodyl supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Bisacodyl manufacturer or Bisacodyl supplier.
PharmaCompass also assists you with knowing the Bisacodyl API Price utilized in the formulation of products. Bisacodyl API Price is not always fixed or binding as the Bisacodyl Price is obtained through a variety of data sources. The Bisacodyl Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A LS-2218 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LS-2218, including repackagers and relabelers. The FDA regulates LS-2218 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LS-2218 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 LS-2218 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A LS-2218 supplier is an individual or a company that provides LS-2218 active pharmaceutical ingredient (API) or LS-2218 finished formulations upon request. The LS-2218 suppliers may include LS-2218 API manufacturers, exporters, distributors and traders.
click here to find a list of LS-2218 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A LS-2218 CEP of the European Pharmacopoeia monograph is often referred to as a LS-2218 Certificate of Suitability (COS). The purpose of a LS-2218 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of LS-2218 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of LS-2218 to their clients by showing that a LS-2218 CEP has been issued for it. The manufacturer submits a LS-2218 CEP (COS) as part of the market authorization procedure, and it takes on the role of a LS-2218 CEP holder for the record. Additionally, the data presented in the LS-2218 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the LS-2218 DMF.
A LS-2218 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. LS-2218 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 LS-2218 suppliers with CEP (COS) on PharmaCompass.
We have 4 companies offering LS-2218
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