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01 1Hubei Goto Biopharm
02 1Yicheng Goto Pharmaceuticals Co Ltd
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01 14-ANDROSTENEDIONE
02 1ANDROSTENEDIONE
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01 2China
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01 2Active
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01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 41649
Submission : 2025-03-31
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31718
Submission : 2017-04-20
Status : Active
Type : II
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PharmaCompass offers a list of Androstenedione 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 Androstenedione manufacturer or Androstenedione supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Androstenedione manufacturer or Androstenedione supplier.
PharmaCompass also assists you with knowing the Androstenedione API Price utilized in the formulation of products. Androstenedione API Price is not always fixed or binding as the Androstenedione Price is obtained through a variety of data sources. The Androstenedione Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A adione manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of adione, including repackagers and relabelers. The FDA regulates adione manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. adione 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 adione supplier is an individual or a company that provides adione active pharmaceutical ingredient (API) or adione finished formulations upon request. The adione suppliers may include adione API manufacturers, exporters, distributors and traders.
click here to find a list of adione suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A adione DMF (Drug Master File) is a document detailing the whole manufacturing process of adione active pharmaceutical ingredient (API) in detail. Different forms of adione DMFs exist exist since differing nations have different regulations, such as adione USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A adione DMF submitted to regulatory agencies in the US is known as a USDMF. adione USDMF includes data on adione's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The adione USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of adione suppliers with USDMF on PharmaCompass.
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