01 1Shionogi Pharma Co., Ltd.
01 1Naldemedine tosylate
01 1Japan
NDC Package Code : 53044-002
Start Marketing Date : 2017-03-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Naldemedine Tosylate 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 Naldemedine Tosylate manufacturer or Naldemedine Tosylate supplier for your needs.
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PharmaCompass also assists you with knowing the Naldemedine Tosylate API Price utilized in the formulation of products. Naldemedine Tosylate API Price is not always fixed or binding as the Naldemedine Tosylate Price is obtained through a variety of data sources. The Naldemedine Tosylate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Naldemedine Tosylate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Naldemedine Tosylate, including repackagers and relabelers. The FDA regulates Naldemedine Tosylate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Naldemedine Tosylate 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 Naldemedine Tosylate supplier is an individual or a company that provides Naldemedine Tosylate active pharmaceutical ingredient (API) or Naldemedine Tosylate finished formulations upon request. The Naldemedine Tosylate suppliers may include Naldemedine Tosylate API manufacturers, exporters, distributors and traders.
click here to find a list of Naldemedine Tosylate 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 Naldemedine Tosylate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Naldemedine Tosylate 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 Naldemedine Tosylate 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 Naldemedine Tosylate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Naldemedine Tosylate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Naldemedine Tosylate suppliers with NDC on PharmaCompass.
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