01 1Curia Spain S.A.U.
02 1Curia Wisconsin, Inc.
01 2Fluoxymesterone
01 2U.S.A
NDC Package Code : 65089-0052
Start Marketing Date : 1983-10-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 64181-0082
Start Marketing Date : 1983-10-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (3kg/3kg)
Marketing Category : BULK INGREDIENT
A Fluoxymesterone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fluoxymesterone, including repackagers and relabelers. The FDA regulates Fluoxymesterone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fluoxymesterone 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 Fluoxymesterone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fluoxymesterone supplier is an individual or a company that provides Fluoxymesterone active pharmaceutical ingredient (API) or Fluoxymesterone finished formulations upon request. The Fluoxymesterone suppliers may include Fluoxymesterone API manufacturers, exporters, distributors and traders.
click here to find a list of Fluoxymesterone 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 Fluoxymesterone as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Fluoxymesterone 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 Fluoxymesterone 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 Fluoxymesterone and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Fluoxymesterone NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Fluoxymesterone suppliers with NDC on PharmaCompass.
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