Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
01 1NURAY CHEMICALS PRIVATE LIMITED
02 1Dr. Reddy's Laboratories Limited
03 1Aurobindo Pharma Limited
04 1Janssen Pharmaceutica NV
05 1Jubilant Biosys limited
06 1STHREE CHEMICALS PRIVATE LIMITED
07 2ScinoPharm Taiwan Ltd.
08 1Teva Czech Industries s.r.o
01 2Benzgalantamine Gluconate
02 1Galantamine
03 3Galantamine Hydrobromide
04 1Galantamine hydrobromide
05 1Galanthamine Hydrobromide
06 1galantamine hydrobromide
01 4India
02 1Israel
03 2Taiwan
04 1U.S.A
05 1Blank
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-134
Start Marketing Date : 2026-05-22
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-081
Start Marketing Date : 2005-01-20
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65862-487
Start Marketing Date : 2024-01-11
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12578-890
Start Marketing Date : 2001-11-15
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65372-1138
Start Marketing Date : 2008-11-28
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65129-1332
Start Marketing Date : 2013-09-02
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65129-1113
Start Marketing Date : 2004-04-29
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 47848-023
Start Marketing Date : 2022-01-26
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 83511-040
Start Marketing Date : 2026-05-22
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
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, 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.
A Galanthamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Galanthamine, including repackagers and relabelers. The FDA regulates Galanthamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Galanthamine 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 Galanthamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Galanthamine supplier is an individual or a company that provides Galanthamine active pharmaceutical ingredient (API) or Galanthamine finished formulations upon request. The Galanthamine suppliers may include Galanthamine API manufacturers, exporters, distributors and traders.
click here to find a list of Galanthamine suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Galanthamine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Galanthamine 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 Galanthamine 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 Galanthamine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Galanthamine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Galanthamine suppliers with NDC on PharmaCompass.
We have 7 companies offering Galanthamine
Get in contact with the supplier of your choice:
