01 1STHREE CHEMICALS PRIVATE LIMITED
02 1Steroid SpA
01 2Oxymetholone
01 1Italy
02 1Blank
NDC Package Code : 49803-008
Start Marketing Date : 2019-10-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25000g/250000g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 83511-011
Start Marketing Date : 2024-12-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
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A Oxymetholone [Androgenic steroids, anabolic] manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxymetholone [Androgenic steroids, anabolic], including repackagers and relabelers. The FDA regulates Oxymetholone [Androgenic steroids, anabolic] manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxymetholone [Androgenic steroids, anabolic] API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Oxymetholone [Androgenic steroids, anabolic] supplier is an individual or a company that provides Oxymetholone [Androgenic steroids, anabolic] active pharmaceutical ingredient (API) or Oxymetholone [Androgenic steroids, anabolic] finished formulations upon request. The Oxymetholone [Androgenic steroids, anabolic] suppliers may include Oxymetholone [Androgenic steroids, anabolic] API manufacturers, exporters, distributors and traders.
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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 Oxymetholone [Androgenic steroids, anabolic] as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Oxymetholone [Androgenic steroids, anabolic] 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 Oxymetholone [Androgenic steroids, anabolic] 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 Oxymetholone [Androgenic steroids, anabolic] and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Oxymetholone [Androgenic steroids, anabolic] NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Oxymetholone [Androgenic steroids, anabolic] suppliers with NDC on PharmaCompass.
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