01 3ABX advanced biochemical compounds Biochemische Forschungsreagenzien GmbH
01 3Iobenguane sulfate
01 3U.S.A
NDC Package Code : 71934-0026
Start Marketing Date : 2023-03-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (100mg/100mg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71934-0027
Start Marketing Date : 2023-03-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (5mg/5mg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71934-0025
Start Marketing Date : 2023-03-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1000mg/1000mg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Iobenguane 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 Iobenguane manufacturer or Iobenguane supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Iobenguane manufacturer or Iobenguane supplier.
PharmaCompass also assists you with knowing the Iobenguane API Price utilized in the formulation of products. Iobenguane API Price is not always fixed or binding as the Iobenguane Price is obtained through a variety of data sources. The Iobenguane Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Iobenguane (sulfate) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iobenguane (sulfate), including repackagers and relabelers. The FDA regulates Iobenguane (sulfate) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iobenguane (sulfate) API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Iobenguane (sulfate) supplier is an individual or a company that provides Iobenguane (sulfate) active pharmaceutical ingredient (API) or Iobenguane (sulfate) finished formulations upon request. The Iobenguane (sulfate) suppliers may include Iobenguane (sulfate) API manufacturers, exporters, distributors and traders.
click here to find a list of Iobenguane (sulfate) 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 Iobenguane (sulfate) as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Iobenguane (sulfate) 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 Iobenguane (sulfate) 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 Iobenguane (sulfate) and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Iobenguane (sulfate) NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Iobenguane (sulfate) suppliers with NDC on PharmaCompass.
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