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.
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 LOA & ddI manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LOA & ddI, including repackagers and relabelers. The FDA regulates LOA & ddI manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LOA & 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.
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A LOA & ddI supplier is an individual or a company that provides LOA & ddI active pharmaceutical ingredient (API) or LOA & ddI finished formulations upon request. The LOA & ddI suppliers may include LOA & ddI API manufacturers, exporters, distributors and traders.
click here to find a list of LOA & ddI suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A LOA & ddI written confirmation (LOA & ddI WC) is an official document issued by a regulatory agency to a LOA & ddI manufacturer, verifying that the manufacturing facility of a LOA & ddI active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting LOA & ddI APIs or LOA & ddI finished pharmaceutical products to another nation, regulatory agencies frequently require a LOA & ddI WC (written confirmation) as part of the regulatory process.
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