01 1ASAHI GLASS CO LTD
02 1Dupont
03 3Blank
01 1PERFLUOROCTYLBROMIDE
02 2PERFLUOROOCTYLBROMIDE
03 1PERFLUOROOCTYLBROMIDE (PFOB), C8F17BR
04 1PERFLUOROOCTYLBROMIDE C8F17Br
01 1Japan
02 1U.S.A
03 3Blank
01 5Inactive
01 5Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8815
Submission : 1990-11-09
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3012
Submission : 1976-06-02
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8503
Submission : 1990-03-23
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9692
Submission : 1992-05-20
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8549
Submission : 1990-05-01
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
47
PharmaCompass offers a list of Perflubron 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 Perflubron manufacturer or Perflubron supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Perflubron manufacturer or Perflubron supplier.
PharmaCompass also assists you with knowing the Perflubron API Price utilized in the formulation of products. Perflubron API Price is not always fixed or binding as the Perflubron Price is obtained through a variety of data sources. The Perflubron Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A LiquiVent manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LiquiVent, including repackagers and relabelers. The FDA regulates LiquiVent manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LiquiVent 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 LiquiVent supplier is an individual or a company that provides LiquiVent active pharmaceutical ingredient (API) or LiquiVent finished formulations upon request. The LiquiVent suppliers may include LiquiVent API manufacturers, exporters, distributors and traders.
click here to find a list of LiquiVent suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A LiquiVent DMF (Drug Master File) is a document detailing the whole manufacturing process of LiquiVent active pharmaceutical ingredient (API) in detail. Different forms of LiquiVent DMFs exist exist since differing nations have different regulations, such as LiquiVent USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A LiquiVent DMF submitted to regulatory agencies in the US is known as a USDMF. LiquiVent USDMF includes data on LiquiVent's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The LiquiVent USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of LiquiVent suppliers with USDMF on PharmaCompass.
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