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01 1ORGAMOL PHARMA SOLUTIONS SA
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01 1SOBREROL
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01 1Switzerland
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01 1Inactive
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01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4905
Submission : 1983-03-23
Status : Inactive
Type : II
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PharmaCompass offers a list of Soberol 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 Soberol manufacturer or Soberol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Soberol manufacturer or Soberol supplier.
PharmaCompass also assists you with knowing the Soberol API Price utilized in the formulation of products. Soberol API Price is not always fixed or binding as the Soberol Price is obtained through a variety of data sources. The Soberol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A sobrerol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of sobrerol, including repackagers and relabelers. The FDA regulates sobrerol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. sobrerol 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 sobrerol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A sobrerol supplier is an individual or a company that provides sobrerol active pharmaceutical ingredient (API) or sobrerol finished formulations upon request. The sobrerol suppliers may include sobrerol API manufacturers, exporters, distributors and traders.
click here to find a list of sobrerol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A sobrerol DMF (Drug Master File) is a document detailing the whole manufacturing process of sobrerol active pharmaceutical ingredient (API) in detail. Different forms of sobrerol DMFs exist exist since differing nations have different regulations, such as sobrerol USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A sobrerol DMF submitted to regulatory agencies in the US is known as a USDMF. sobrerol USDMF includes data on sobrerol's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The sobrerol USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of sobrerol suppliers with USDMF on PharmaCompass.
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