01 1M/s. Aurobindo Pharma Ltd., (Unit-XI),
02 1 M/s. Aurobindo Pharma Ltd.
01 1Amoxicillin Trihydrate (Ph. Eur)
02 1Amoxicillin Trihydrate EP
01 1WC-0023
02 1WC-0121
01 2India
Date of Issue : 2019-07-05
Valid Till : 2022-07-02
Written Confirmation Number : WC-0121
Address of the Firm : Unit-V, Plot No.79-91, IDA, Chemical Zone, Pashamylaram (V), Patancheru (M), Med...
Amoxicillin Trihydrate (Ph. Eur)
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 Amoxicillin Trihydrate 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 Amoxicillin Trihydrate manufacturer or Amoxicillin Trihydrate supplier for your needs.
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PharmaCompass also assists you with knowing the Amoxicillin Trihydrate API Price utilized in the formulation of products. Amoxicillin Trihydrate API Price is not always fixed or binding as the Amoxicillin Trihydrate Price is obtained through a variety of data sources. The Amoxicillin Trihydrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DisperMox manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DisperMox, including repackagers and relabelers. The FDA regulates DisperMox manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DisperMox 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 DisperMox supplier is an individual or a company that provides DisperMox active pharmaceutical ingredient (API) or DisperMox finished formulations upon request. The DisperMox suppliers may include DisperMox API manufacturers, exporters, distributors and traders.
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A DisperMox written confirmation (DisperMox WC) is an official document issued by a regulatory agency to a DisperMox manufacturer, verifying that the manufacturing facility of a DisperMox active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting DisperMox APIs or DisperMox finished pharmaceutical products to another nation, regulatory agencies frequently require a DisperMox WC (written confirmation) as part of the regulatory process.
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