01 1Curia Spain S.A.U.
02 1zhejiang xianju pharmaceutical co., Ltd.
01 1Brexanolone
02 1brexanolone
01 1China
02 1U.S.A
NDC Package Code : 65089-0060
Start Marketing Date : 2021-02-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 60722-3015
Start Marketing Date : 2022-07-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Brexanolone 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 Brexanolone manufacturer or Brexanolone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Brexanolone manufacturer or Brexanolone supplier.
PharmaCompass also assists you with knowing the Brexanolone API Price utilized in the formulation of products. Brexanolone API Price is not always fixed or binding as the Brexanolone Price is obtained through a variety of data sources. The Brexanolone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A (3a)-Allopregnanolone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (3a)-Allopregnanolone, including repackagers and relabelers. The FDA regulates (3a)-Allopregnanolone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (3a)-Allopregnanolone 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 (3a)-Allopregnanolone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A (3a)-Allopregnanolone supplier is an individual or a company that provides (3a)-Allopregnanolone active pharmaceutical ingredient (API) or (3a)-Allopregnanolone finished formulations upon request. The (3a)-Allopregnanolone suppliers may include (3a)-Allopregnanolone API manufacturers, exporters, distributors and traders.
click here to find a list of (3a)-Allopregnanolone 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 (3a)-Allopregnanolone as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for (3a)-Allopregnanolone 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 (3a)-Allopregnanolone 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 (3a)-Allopregnanolone and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a (3a)-Allopregnanolone NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of (3a)-Allopregnanolone suppliers with NDC on PharmaCompass.
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