01 1Alivira Animal Health Limited
01 1FLUBENDAZOLE
01 1India
NDC Package Code : 86055-0027
Start Marketing Date : 2022-11-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Flubendazole manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flubendazole, including repackagers and relabelers. The FDA regulates Flubendazole manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flubendazole 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 Flubendazole manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Flubendazole supplier is an individual or a company that provides Flubendazole active pharmaceutical ingredient (API) or Flubendazole finished formulations upon request. The Flubendazole suppliers may include Flubendazole API manufacturers, exporters, distributors and traders.
click here to find a list of Flubendazole 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 Flubendazole as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Flubendazole 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 Flubendazole 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 Flubendazole and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Flubendazole NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Flubendazole suppliers with NDC on PharmaCompass.
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