01 2Derivados Quimicos
01 1Butoconazole Nitrate
02 1Butoconazole nitrate micronized
01 2Spain
NDC Package Code : 59349-0034
Start Marketing Date : 2023-03-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59349-0006
Start Marketing Date : 2018-11-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Butoconazole Nitrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Butoconazole Nitrate, including repackagers and relabelers. The FDA regulates Butoconazole Nitrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Butoconazole Nitrate 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 Butoconazole Nitrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Butoconazole Nitrate supplier is an individual or a company that provides Butoconazole Nitrate active pharmaceutical ingredient (API) or Butoconazole Nitrate finished formulations upon request. The Butoconazole Nitrate suppliers may include Butoconazole Nitrate API manufacturers, exporters, distributors and traders.
click here to find a list of Butoconazole Nitrate 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 Butoconazole Nitrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Butoconazole Nitrate 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 Butoconazole Nitrate 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 Butoconazole Nitrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Butoconazole Nitrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Butoconazole Nitrate suppliers with NDC on PharmaCompass.
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