01 1M/s. Aurobindo Pharma Ltd., (Unit-XI),
01 1Didanosine (Ph. Eur)
01 1WC-0023
01 1India
Date of Issue : 2019-06-26
Valid Till : 2022-06-25
Written Confirmation Number : WC-0023
Address of the Firm : Sy.No.1/22, 2/1 To 5, 6 to 18, 61 to 69, Pydibhimavaram Village, Ranasthalam, Sr...
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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.
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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 written confirmation (DDI WC) is an official document issued by a regulatory agency to a DDI manufacturer, verifying that the manufacturing facility of a DDI active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting DDI APIs or DDI finished pharmaceutical products to another nation, regulatory agencies frequently require a DDI WC (written confirmation) as part of the regulatory process.
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