Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
01 1Rusan Pharma Ltd
02 1FRANCOPIA
03 1Sanofi Winthrop Industrie
04 1LETCO MEDICAL, LLC
05 1MAEDA INC
06 1Professional Compounding Centers of America dba PCCA
07 1SpecGx LLC
01 4NALBUPHINE HYDROCHLORIDE
02 3Nalbuphine Hydrochloride
01 2France
02 1India
03 1Ireland
04 1U.S.A
05 1United Kingdom
06 1Blank
Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
NDC Package Code : 70312-0891
Start Marketing Date : 2026-04-08
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
NDC Package Code : 50396-0201
Start Marketing Date : 2018-06-19
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
NDC Package Code : 52465-106
Start Marketing Date : 2018-06-19
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-1546
Start Marketing Date : 2010-11-17
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 0406-3360
Start Marketing Date : 2010-06-25
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-2140
Start Marketing Date : 2013-06-20
End Marketing Date : 2028-02-28
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 86184-262
Start Marketing Date : 2026-03-27
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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A Nalbufina clorhidrato manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nalbufina clorhidrato, including repackagers and relabelers. The FDA regulates Nalbufina clorhidrato manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nalbufina clorhidrato 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 Nalbufina clorhidrato supplier is an individual or a company that provides Nalbufina clorhidrato active pharmaceutical ingredient (API) or Nalbufina clorhidrato finished formulations upon request. The Nalbufina clorhidrato suppliers may include Nalbufina clorhidrato 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 Nalbufina clorhidrato as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Nalbufina clorhidrato 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 Nalbufina clorhidrato 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 Nalbufina clorhidrato and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Nalbufina clorhidrato NDC to their finished compounded human drug products, they may choose to do so.
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