01 1GE Healthcare Lindesnes
01 1Gadodiamide
01 1United Kingdom
NDC Package Code : 71806-069
Start Marketing Date : 1993-01-08
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Gadodiamide 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 Gadodiamide manufacturer or Gadodiamide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Gadodiamide manufacturer or Gadodiamide supplier.
PharmaCompass also assists you with knowing the Gadodiamide API Price utilized in the formulation of products. Gadodiamide API Price is not always fixed or binding as the Gadodiamide Price is obtained through a variety of data sources. The Gadodiamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Gd-DTPA-BMA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gd-DTPA-BMA, including repackagers and relabelers. The FDA regulates Gd-DTPA-BMA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gd-DTPA-BMA 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 Gd-DTPA-BMA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Gd-DTPA-BMA supplier is an individual or a company that provides Gd-DTPA-BMA active pharmaceutical ingredient (API) or Gd-DTPA-BMA finished formulations upon request. The Gd-DTPA-BMA suppliers may include Gd-DTPA-BMA API manufacturers, exporters, distributors and traders.
click here to find a list of Gd-DTPA-BMA 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 Gd-DTPA-BMA as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Gd-DTPA-BMA 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 Gd-DTPA-BMA 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 Gd-DTPA-BMA and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Gd-DTPA-BMA NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Gd-DTPA-BMA suppliers with NDC on PharmaCompass.
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