01 1Aurobindo Pharma Limited
02 1Janssen Pharmaceutica NV
03 1Jubilant Pharmova Limited
04 2ScinoPharm Taiwan Ltd.
05 1Teva Czech Industries s.r.o
01 1Galantamine
02 2Galantamine Hydrobromide
03 1Galantamine hydrobromide
04 1Galanthamine Hydrobromide
05 1galantamine hydrobromide
01 2India
02 1Israel
03 2Taiwan
04 1U.S.A
NDC Package Code : 65862-487
Start Marketing Date : 2024-01-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12578-890
Start Marketing Date : 2001-11-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65372-1138
Start Marketing Date : 2008-11-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65129-1113
Start Marketing Date : 2004-04-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65129-1332
Start Marketing Date : 2013-09-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 47848-023
Start Marketing Date : 2022-01-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Galantamine Hydrobromide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Galantamine Hydrobromide manufacturer or Galantamine Hydrobromide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Galantamine Hydrobromide manufacturer or Galantamine Hydrobromide supplier.
PharmaCompass also assists you with knowing the Galantamine Hydrobromide API Price utilized in the formulation of products. Galantamine Hydrobromide API Price is not always fixed or binding as the Galantamine Hydrobromide Price is obtained through a variety of data sources. The Galantamine Hydrobromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Nivalin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nivalin, including repackagers and relabelers. The FDA regulates Nivalin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nivalin 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 Nivalin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nivalin supplier is an individual or a company that provides Nivalin active pharmaceutical ingredient (API) or Nivalin finished formulations upon request. The Nivalin suppliers may include Nivalin API manufacturers, exporters, distributors and traders.
click here to find a list of Nivalin 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 Nivalin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Nivalin 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 Nivalin 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 Nivalin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Nivalin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Nivalin suppliers with NDC on PharmaCompass.
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