01 1M/s Vital Laboratories Pvt ltd
01 1Piperazine Citrate EP
01 1WC-0300
01 1India
Date of Issue : 2024-05-20
Valid Till : 2027-01-08
Written Confirmation Number : WC-0300
Address of the Firm : Plot No. 1710, Phase-lll, G.I.D.C Estate, Vapi-396195, Dist.-Valsad, Gujarat, In...
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PharmaCompass offers a list of Piperazine Citrate 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 Piperazine Citrate manufacturer or Piperazine Citrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Piperazine Citrate manufacturer or Piperazine Citrate supplier.
PharmaCompass also assists you with knowing the Piperazine Citrate API Price utilized in the formulation of products. Piperazine Citrate API Price is not always fixed or binding as the Piperazine Citrate Price is obtained through a variety of data sources. The Piperazine Citrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DAK 63 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DAK 63, including repackagers and relabelers. The FDA regulates DAK 63 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DAK 63 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 DAK 63 supplier is an individual or a company that provides DAK 63 active pharmaceutical ingredient (API) or DAK 63 finished formulations upon request. The DAK 63 suppliers may include DAK 63 API manufacturers, exporters, distributors and traders.
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A DAK 63 written confirmation (DAK 63 WC) is an official document issued by a regulatory agency to a DAK 63 manufacturer, verifying that the manufacturing facility of a DAK 63 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting DAK 63 APIs or DAK 63 finished pharmaceutical products to another nation, regulatory agencies frequently require a DAK 63 WC (written confirmation) as part of the regulatory process.
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