01 2Asclemed USA, Inc.
02 1Bayer de Mexico, S.A. de C.V.
03 1Brichem Sciences Private Limited
04 1Hubei Zhuxi Humanwell Pharmaceutical Co., Ltd.
05 3Jiangsu Jiaerke Pharmaceuticals Group Corp., Ltd.
06 2LETCO MEDICAL, LLC
07 1Medisca Inc.
08 2Pharma Source Direct, Inc.
09 1Professional Compounding Centers of America dba PCCA
10 1SCH Global Services Private Limited
01 1DEHYDROEPIANDROSTERONE
02 1DHEA (Prasterone)
03 2Dehydroepiandrosterone
04 1Dehydroepiandrosterone (DHEA)
05 1Dehydroepiandrosterone (Micronized) (DHEA)
06 2Dehydroepiandrosterone IH
07 1Dehydroepiandrosterone Non-Micronized
08 4PRASTERONE
09 1Prasterone
10 1dehydroepiandrosterone
01 4China
02 7U.S.A
03 1United Kingdom
04 3Blank
NDC Package Code : 76420-688
Start Marketing Date : 2018-06-21
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (0.04g/g)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 70492-004
Start Marketing Date : 2018-09-30
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 64025-0017
Start Marketing Date : 2005-03-04
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 64025-0022
Start Marketing Date : 2023-09-15
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 64025-0015
Start Marketing Date : 2009-12-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-3205
Start Marketing Date : 2024-01-09
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-3188
Start Marketing Date : 2023-04-17
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-0733
Start Marketing Date : 2007-02-13
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-2960
Start Marketing Date : 2020-06-29
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 12875-9930
Start Marketing Date : 2011-03-15
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Portfolio PDF
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PharmaCompass offers a list of Prasterone API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Prasterone manufacturer or Prasterone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Prasterone manufacturer or Prasterone supplier.
A Dehydro-epi-androsterone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dehydro-epi-androsterone, including repackagers and relabelers. The FDA regulates Dehydro-epi-androsterone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dehydro-epi-androsterone 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 Dehydro-epi-androsterone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Dehydro-epi-androsterone supplier is an individual or a company that provides Dehydro-epi-androsterone active pharmaceutical ingredient (API) or Dehydro-epi-androsterone finished formulations upon request. The Dehydro-epi-androsterone suppliers may include Dehydro-epi-androsterone API manufacturers, exporters, distributors and traders.
click here to find a list of Dehydro-epi-androsterone suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Dehydro-epi-androsterone as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Dehydro-epi-androsterone 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 Dehydro-epi-androsterone 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 Dehydro-epi-androsterone and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Dehydro-epi-androsterone NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Dehydro-epi-androsterone suppliers with NDC on PharmaCompass.
We have 7 companies offering Dehydro-epi-androsterone
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