Veranova: A CDMO that manages complexity with confidence.
01 2Veranova, L.P.
02 1Medisca Inc.
03 1Pharma Source Direct, Inc.
04 1Professional Compounding Centers of America dba PCCA
05 4SpecGx LLC
01 2SUFENTANIL
02 2SUFENTANIL CITRATE
03 1Sufentanil Base
04 4Sufentanil Citrate
01 4Ireland
02 4U.S.A
03 1United Kingdom
Veranova: A CDMO that manages complexity with confidence.
NDC Package Code : 49812-0021
Start Marketing Date : 1995-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Veranova: A CDMO that manages complexity with confidence.
NDC Package Code : 49812-0110
Start Marketing Date : 2005-06-09
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (50g/50g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0406-0678
Start Marketing Date : 2017-01-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 0406-0310
Start Marketing Date : 2013-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0406-0330
Start Marketing Date : 2013-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0406-0672
Start Marketing Date : 2013-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-1968
Start Marketing Date : 2012-11-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-3213
Start Marketing Date : 2002-07-19
End Marketing Date : 2028-06-30
Dosage Form (Strength) : POWDER (1mg/mg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 82393-121
Start Marketing Date : 2022-01-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
A Sufentanil Citrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sufentanil Citrate, including repackagers and relabelers. The FDA regulates Sufentanil Citrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sufentanil Citrate 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 Sufentanil Citrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sufentanil Citrate supplier is an individual or a company that provides Sufentanil Citrate active pharmaceutical ingredient (API) or Sufentanil Citrate finished formulations upon request. The Sufentanil Citrate suppliers may include Sufentanil Citrate API manufacturers, exporters, distributors and traders.
click here to find a list of Sufentanil Citrate 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 Sufentanil Citrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sufentanil Citrate 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 Sufentanil Citrate 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 Sufentanil Citrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sufentanil Citrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sufentanil Citrate suppliers with NDC on PharmaCompass.
We have 5 companies offering Sufentanil Citrate
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