Veranova: A CDMO that manages complexity with confidence.
01 1Veranova, L.P.
02 1Cambrex Charles City, Inc
03 1Chattem Chemicals, Inc.
04 1Curia Missouri, Inc.
05 1Curia New York, Inc.
06 1Siegfried USA, LLC
01 2Gamma Hydroxybutyric Acid
02 4Sodium Oxybate
01 1Switzerland
02 5U.S.A
Veranova: A CDMO that manages complexity with confidence.
NDC Package Code : 49812-0207
Start Marketing Date : 2010-06-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59116-5950
Start Marketing Date : 2021-12-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 61960-0221
Start Marketing Date : 2017-12-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17180-2010
Start Marketing Date : 2002-07-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (13kg/13kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 65392-3417
Start Marketing Date : 2002-07-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0792-4356
Start Marketing Date : 2011-05-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A Sodium Oxybate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Oxybate, including repackagers and relabelers. The FDA regulates Sodium Oxybate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Oxybate 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 Sodium Oxybate supplier is an individual or a company that provides Sodium Oxybate active pharmaceutical ingredient (API) or Sodium Oxybate finished formulations upon request. The Sodium Oxybate suppliers may include Sodium Oxybate 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 Sodium Oxybate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sodium Oxybate 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 Sodium Oxybate 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 Sodium Oxybate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sodium Oxybate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sodium Oxybate suppliers with NDC on PharmaCompass.
We have 5 companies offering Sodium Oxybate
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