01 1Fagron Inc
02 1Fagron Services BV
03 1Hubei Gedian Humanwell Pharmaceutical Co., Ltd.
04 1Hubei Zhuxi Humanwell Pharmaceutical Co., Ltd.
05 2Jiangsu Jiaerke Pharmaceuticals Group Corp., Ltd.
06 1Kalchem International inc
07 2Medisca Inc.
08 2Pharma Source Direct, Inc.
09 1Professional Compounding Centers of America dba PCCA
01 2PREGNENOLONE
02 7Pregnenolone
03 1Pregnenolone (Micronized)
04 1Pregnenolone Acetate
05 1Pregnenolone Micro
01 4China
02 2Netherlands
03 5U.S.A
04 1United Kingdom
NDC Package Code : 76003-1501
Start Marketing Date : 2010-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51552-0757
Start Marketing Date : 1998-04-01
End Marketing Date : 2025-04-03
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 70492-003
Start Marketing Date : 2018-09-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51508-003
Start Marketing Date : 2013-02-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 64025-0012
Start Marketing Date : 2009-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 64025-0014
Start Marketing Date : 2009-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60592-072
Start Marketing Date : 2020-01-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0769
Start Marketing Date : 2013-08-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-2233
Start Marketing Date : 2006-08-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-5195
Start Marketing Date : 2022-10-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
A Pregnenolone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pregnenolone, including repackagers and relabelers. The FDA regulates Pregnenolone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pregnenolone 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 Pregnenolone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pregnenolone supplier is an individual or a company that provides Pregnenolone active pharmaceutical ingredient (API) or Pregnenolone finished formulations upon request. The Pregnenolone suppliers may include Pregnenolone API manufacturers, exporters, distributors and traders.
click here to find a list of Pregnenolone 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 Pregnenolone as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Pregnenolone 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 Pregnenolone 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 Pregnenolone and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Pregnenolone NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Pregnenolone suppliers with NDC on PharmaCompass.
We have 7 companies offering Pregnenolone
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