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 2MSN Organics Private Limited
03 1SMS Pharmaceuticals Limited
04 1TAPI Czech Industries s.r.o.
05 1Teva Czech Industries s.r.o
01 1PERAMPANEL
02 4Perampanel
03 1Perampanel (3/4 Hydrate)
01 4India
02 1Israel
03 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 : 58159-099
Start Marketing Date : 2023-12-06
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50379-0020
Start Marketing Date : 2016-10-03
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50379-0024
Start Marketing Date : 2021-01-29
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 67835-0026
Start Marketing Date : 2021-09-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 47848-049
Start Marketing Date : 2014-04-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 84644-049
Start Marketing Date : 2014-04-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
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A Fycompa manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fycompa, including repackagers and relabelers. The FDA regulates Fycompa manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fycompa 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 Fycompa manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fycompa supplier is an individual or a company that provides Fycompa active pharmaceutical ingredient (API) or Fycompa finished formulations upon request. The Fycompa suppliers may include Fycompa API manufacturers, exporters, distributors and traders.
click here to find a list of Fycompa 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 Fycompa as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Fycompa 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 Fycompa 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 Fycompa and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Fycompa NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Fycompa suppliers with NDC on PharmaCompass.
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