01 1M/s Glenmark life Sciences limited
01 1Deoxycholic Acid USP
01 1WC-0310
01 1India
Date of Issue : 2023-11-28
Valid Till : 2026-11-28
Written Confirmation Number : WC-0310
Address of the Firm : Plot No. Z-103/l, Dahej SEZ, Phase II, Dahej, Dist-Bharuch, Gujarat, India
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PharmaCompass offers a list of Deoxycholic Acid 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 Deoxycholic Acid manufacturer or Deoxycholic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Deoxycholic Acid manufacturer or Deoxycholic Acid supplier.
PharmaCompass also assists you with knowing the Deoxycholic Acid API Price utilized in the formulation of products. Deoxycholic Acid API Price is not always fixed or binding as the Deoxycholic Acid Price is obtained through a variety of data sources. The Deoxycholic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A KYBELLA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of KYBELLA, including repackagers and relabelers. The FDA regulates KYBELLA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. KYBELLA 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 KYBELLA supplier is an individual or a company that provides KYBELLA active pharmaceutical ingredient (API) or KYBELLA finished formulations upon request. The KYBELLA suppliers may include KYBELLA API manufacturers, exporters, distributors and traders.
click here to find a list of KYBELLA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A KYBELLA written confirmation (KYBELLA WC) is an official document issued by a regulatory agency to a KYBELLA manufacturer, verifying that the manufacturing facility of a KYBELLA active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting KYBELLA APIs or KYBELLA finished pharmaceutical products to another nation, regulatory agencies frequently require a KYBELLA WC (written confirmation) as part of the regulatory process.
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