01 2Erregierre SpA
02 1Solara Active Pharma Sciences Limited
01 3Tioconazole
01 1India
02 2Italy
NDC Package Code : 49706-1282
Start Marketing Date : 2010-01-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49706-1283
Start Marketing Date : 2010-01-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 72643-029
Start Marketing Date : 2022-07-06
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Tioconazole manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tioconazole, including repackagers and relabelers. The FDA regulates Tioconazole manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tioconazole 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 Tioconazole manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tioconazole supplier is an individual or a company that provides Tioconazole active pharmaceutical ingredient (API) or Tioconazole finished formulations upon request. The Tioconazole suppliers may include Tioconazole API manufacturers, exporters, distributors and traders.
click here to find a list of Tioconazole 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 Tioconazole as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Tioconazole 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 Tioconazole 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 Tioconazole and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tioconazole NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Tioconazole suppliers with NDC on PharmaCompass.
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