01 1Edmond Pharma Srl
01 1Noradrenaline Bitartrate Monohydrate
01 1Sweden
NDC Package Code : 66583-0520
Start Marketing Date : 2016-06-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A Abbott Brand of Levophed Bitartrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Abbott Brand of Levophed Bitartrate, including repackagers and relabelers. The FDA regulates Abbott Brand of Levophed Bitartrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Abbott Brand of Levophed Bitartrate 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 Abbott Brand of Levophed Bitartrate supplier is an individual or a company that provides Abbott Brand of Levophed Bitartrate active pharmaceutical ingredient (API) or Abbott Brand of Levophed Bitartrate finished formulations upon request. The Abbott Brand of Levophed Bitartrate suppliers may include Abbott Brand of Levophed Bitartrate API manufacturers, exporters, distributors and traders.
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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 Abbott Brand of Levophed Bitartrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Abbott Brand of Levophed Bitartrate 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 Abbott Brand of Levophed Bitartrate 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 Abbott Brand of Levophed Bitartrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Abbott Brand of Levophed Bitartrate NDC to their finished compounded human drug products, they may choose to do so.
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