01 1APICORE PHARMACEUTICALS PRIVATE LIMITED
02 1HETERO LABS LIMITED
03 1Hetero Labs Limited
04 1Lundbeck Pharmaceuticals Italy S.p.A.
05 2MSN Pharmachem Private Limited
06 1Symed Labs Limited
07 1Unichem Laboratories Limited, India
01 1VORTIOXETINE HYDROBROMIDE
02 7Vortioxetine Hydrobromide
01 1Denmark
02 7India
NDC Package Code : 42973-236
Start Marketing Date : 2017-06-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 45562-1135
Start Marketing Date : 2013-12-05
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 68554-0110
Start Marketing Date : 2013-09-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 68554-0151
Start Marketing Date : 2013-09-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50370-0051
Start Marketing Date : 2015-10-21
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50370-0054
Start Marketing Date : 2017-02-16
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66022-0211
Start Marketing Date : 2023-09-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53747-072
Start Marketing Date : 2017-03-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Vortioxetine Hydrobromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vortioxetine Hydrobromide, including repackagers and relabelers. The FDA regulates Vortioxetine Hydrobromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vortioxetine Hydrobromide 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 Vortioxetine Hydrobromide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vortioxetine Hydrobromide supplier is an individual or a company that provides Vortioxetine Hydrobromide active pharmaceutical ingredient (API) or Vortioxetine Hydrobromide finished formulations upon request. The Vortioxetine Hydrobromide suppliers may include Vortioxetine Hydrobromide API manufacturers, exporters, distributors and traders.
click here to find a list of Vortioxetine Hydrobromide 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 Vortioxetine Hydrobromide as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Vortioxetine Hydrobromide 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 Vortioxetine Hydrobromide 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 Vortioxetine Hydrobromide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Vortioxetine Hydrobromide NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Vortioxetine Hydrobromide suppliers with NDC on PharmaCompass.
We have 6 companies offering Vortioxetine Hydrobromide
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