Experts in producing high-quality APIs from natural sources, specializing in advanced extraction and isolation techniques.
01 1Phytex Australia Pty Ltd
01 1Castanospermine
01 1Australia
Experts in producing high-quality APIs from natural sources, specializing in advanced extraction and isolation techniques.
NDC Package Code : 51886-1001
Start Marketing Date : 1994-04-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Castanospermine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Castanospermine, including repackagers and relabelers. The FDA regulates Castanospermine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Castanospermine 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 Castanospermine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Castanospermine supplier is an individual or a company that provides Castanospermine active pharmaceutical ingredient (API) or Castanospermine finished formulations upon request. The Castanospermine suppliers may include Castanospermine API manufacturers, exporters, distributors and traders.
click here to find a list of Castanospermine 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 Castanospermine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Castanospermine 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 Castanospermine 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 Castanospermine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Castanospermine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Castanospermine suppliers with NDC on PharmaCompass.
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