01 1Air Liquide Healthcare America Corp.
02 1FLUOROMED LP
03 1GE Healthcare Inc
01 199M TC-PERTECHNETATE-SULFUR COLLOID
02 1SULFUR HEXAFLUORIDE (SF6) GAS
03 1SULFUR HEXAFLUORIDE, 99.8%
01 2U.S.A
02 1United Kingdom
01 2Active
02 1Inactive
01 3Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15094
Submission : 2000-10-13
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37317
Submission : 2023-03-24
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1888
Submission : 1972-03-08
Status : Inactive
Type : II
85
PharmaCompass offers a list of Sulfur Hexafluoride 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 Sulfur Hexafluoride manufacturer or Sulfur Hexafluoride supplier for your needs.
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PharmaCompass also assists you with knowing the Sulfur Hexafluoride API Price utilized in the formulation of products. Sulfur Hexafluoride API Price is not always fixed or binding as the Sulfur Hexafluoride Price is obtained through a variety of data sources. The Sulfur Hexafluoride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A UN1080 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of UN1080, including repackagers and relabelers. The FDA regulates UN1080 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. UN1080 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 UN1080 supplier is an individual or a company that provides UN1080 active pharmaceutical ingredient (API) or UN1080 finished formulations upon request. The UN1080 suppliers may include UN1080 API manufacturers, exporters, distributors and traders.
click here to find a list of UN1080 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A UN1080 DMF (Drug Master File) is a document detailing the whole manufacturing process of UN1080 active pharmaceutical ingredient (API) in detail. Different forms of UN1080 DMFs exist exist since differing nations have different regulations, such as UN1080 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A UN1080 DMF submitted to regulatory agencies in the US is known as a USDMF. UN1080 USDMF includes data on UN1080's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The UN1080 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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