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 : 2025-12-31
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 : 2026-12-31
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 Oxybutyrate, Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxybutyrate, Sodium, including repackagers and relabelers. The FDA regulates Oxybutyrate, Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxybutyrate, Sodium 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 Oxybutyrate, Sodium supplier is an individual or a company that provides Oxybutyrate, Sodium active pharmaceutical ingredient (API) or Oxybutyrate, Sodium finished formulations upon request. The Oxybutyrate, Sodium suppliers may include Oxybutyrate, Sodium 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 Oxybutyrate, Sodium as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Oxybutyrate, Sodium 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 Oxybutyrate, Sodium 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 Oxybutyrate, Sodium and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Oxybutyrate, Sodium NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Oxybutyrate, Sodium suppliers with NDC on PharmaCompass.
We have 5 companies offering Oxybutyrate, Sodium
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