01 2Eli Lilly Kinsale Limited
01 2Lasmiditan hemisuccinate
01 2U.S.A
NDC Package Code : 63419-0576
Start Marketing Date : 2018-12-10
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63419-0580
Start Marketing Date : 2020-11-15
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Lasmiditan Succinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lasmiditan Succinate, including repackagers and relabelers. The FDA regulates Lasmiditan Succinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lasmiditan Succinate 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 Lasmiditan Succinate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lasmiditan Succinate supplier is an individual or a company that provides Lasmiditan Succinate active pharmaceutical ingredient (API) or Lasmiditan Succinate finished formulations upon request. The Lasmiditan Succinate suppliers may include Lasmiditan Succinate API manufacturers, exporters, distributors and traders.
click here to find a list of Lasmiditan Succinate 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 Lasmiditan Succinate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Lasmiditan Succinate 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 Lasmiditan Succinate 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 Lasmiditan Succinate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Lasmiditan Succinate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Lasmiditan Succinate suppliers with NDC on PharmaCompass.
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