01 2F2 Chemicals
01 2PERFLUOROBUTANE
01 2United Kingdom
01 1Active
02 1Inactive
01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20864
Submission : 2007-09-28
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15166
Submission : 2000-11-14
Status : Inactive
Type : II
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PharmaCompass offers a list of Perfluorobutane 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 Perfluorobutane manufacturer or Perfluorobutane supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Perfluorobutane manufacturer or Perfluorobutane supplier.
PharmaCompass also assists you with knowing the Perfluorobutane API Price utilized in the formulation of products. Perfluorobutane API Price is not always fixed or binding as the Perfluorobutane Price is obtained through a variety of data sources. The Perfluorobutane Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CEA 410 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CEA 410, including repackagers and relabelers. The FDA regulates CEA 410 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CEA 410 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 CEA 410 supplier is an individual or a company that provides CEA 410 active pharmaceutical ingredient (API) or CEA 410 finished formulations upon request. The CEA 410 suppliers may include CEA 410 API manufacturers, exporters, distributors and traders.
click here to find a list of CEA 410 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A CEA 410 DMF (Drug Master File) is a document detailing the whole manufacturing process of CEA 410 active pharmaceutical ingredient (API) in detail. Different forms of CEA 410 DMFs exist exist since differing nations have different regulations, such as CEA 410 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A CEA 410 DMF submitted to regulatory agencies in the US is known as a USDMF. CEA 410 USDMF includes data on CEA 410's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The CEA 410 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of CEA 410 suppliers with USDMF on PharmaCompass.
