01 1AUROBINDO PHARMA LIMITED Hyderabad IN
02 1MYLAN LABORATORIES LIMITED Hyderabad IN
01 2Didanosine
01 1India
02 1U.S.A
01 1Valid
02 1Withdrawn by Holder
Certificate Number : R1-CEP 2007-301 - Rev 02
Status : Valid
Issue Date : 2017-02-03
Type : Chemical
Substance Number : 2200
Certificate Number : R0-CEP 2013-356 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2017-09-18
Type : Chemical
Substance Number : 2200
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PharmaCompass offers a list of Didanosine 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 Didanosine manufacturer or Didanosine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Didanosine manufacturer or Didanosine supplier.
PharmaCompass also assists you with knowing the Didanosine API Price utilized in the formulation of products. Didanosine API Price is not always fixed or binding as the Didanosine Price is obtained through a variety of data sources. The Didanosine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DDI manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DDI, including repackagers and relabelers. The FDA regulates DDI manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DDI 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 DDI manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DDI supplier is an individual or a company that provides DDI active pharmaceutical ingredient (API) or DDI finished formulations upon request. The DDI suppliers may include DDI API manufacturers, exporters, distributors and traders.
click here to find a list of DDI suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DDI CEP of the European Pharmacopoeia monograph is often referred to as a DDI Certificate of Suitability (COS). The purpose of a DDI CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of DDI EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of DDI to their clients by showing that a DDI CEP has been issued for it. The manufacturer submits a DDI CEP (COS) as part of the market authorization procedure, and it takes on the role of a DDI CEP holder for the record. Additionally, the data presented in the DDI CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the DDI DMF.
A DDI CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. DDI 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 DDI suppliers with CEP (COS) on PharmaCompass.
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