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01 Curia New York, Inc. (2)
02 MAEDA INC (1)
01 VORINOSTAT (1)
02 Vorinostat Coarse (1)
03 Vorinostat Fine (1)
01 U.S.A (2)
02 Blank (1)
13
PharmaCompass offers a list of Vorinostat 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 Vorinostat manufacturer or Vorinostat supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vorinostat manufacturer or Vorinostat supplier.
PharmaCompass also assists you with knowing the Vorinostat API Price utilized in the formulation of products. Vorinostat API Price is not always fixed or binding as the Vorinostat Price is obtained through a variety of data sources. The Vorinostat Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AM20030018 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AM20030018, including repackagers and relabelers. The FDA regulates AM20030018 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AM20030018 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 AM20030018 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AM20030018 supplier is an individual or a company that provides AM20030018 active pharmaceutical ingredient (API) or AM20030018 finished formulations upon request. The AM20030018 suppliers may include AM20030018 API manufacturers, exporters, distributors and traders.
click here to find a list of AM20030018 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing AM20030018 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for AM20030018 API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture AM20030018 as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain AM20030018 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a AM20030018 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of AM20030018 suppliers with NDC on PharmaCompass.
