01 1Qingdao Biopeptek Co., Ltd.
01 1MK-2866
01 1U.S.A
NDC Package Code : 73212-082
Start Marketing Date : 2023-11-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Enobosarm API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Enobosarm manufacturer or Enobosarm supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Enobosarm manufacturer or Enobosarm supplier.
PharmaCompass also assists you with knowing the Enobosarm API Price utilized in the formulation of products. Enobosarm API Price is not always fixed or binding as the Enobosarm Price is obtained through a variety of data sources. The Enobosarm Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Enobosarm manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Enobosarm, including repackagers and relabelers. The FDA regulates Enobosarm manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Enobosarm API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Enobosarm supplier is an individual or a company that provides Enobosarm active pharmaceutical ingredient (API) or Enobosarm finished formulations upon request. The Enobosarm suppliers may include Enobosarm API manufacturers, exporters, distributors and traders.
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 Enobosarm as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Enobosarm 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 Enobosarm 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 Enobosarm and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Enobosarm NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Enobosarm suppliers with NDC on PharmaCompass.
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