01 1F.I.S. Fabbrica Italiana Sintetici
02 1HESS & CLARK INC
03 1Medimpex
01 1FURAZOLIDONE
02 1FURAZOLIDONE BULK
03 1USE OF FURAZOLIDONE TO MEDICATE DUCKS (VET)
01 1Italy
02 1U.S.A
03 1United Kingdom
01 3Inactive
01 3Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4338
Submission : 1981-10-16
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 774
Submission : 1964-01-14
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4060
Submission : 1981-02-17
Status : Inactive
Type : II
56
PharmaCompass offers a list of Furazolidone 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 Furazolidone manufacturer or Furazolidone supplier for your needs.
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A 3-{[(5-nitro-2-furyl)methylene]amino}-1,3-oxazolidin-2-one manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 3-{[(5-nitro-2-furyl)methylene]amino}-1,3-oxazolidin-2-one, including repackagers and relabelers. The FDA regulates 3-{[(5-nitro-2-furyl)methylene]amino}-1,3-oxazolidin-2-one manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 3-{[(5-nitro-2-furyl)methylene]amino}-1,3-oxazolidin-2-one API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A 3-{[(5-nitro-2-furyl)methylene]amino}-1,3-oxazolidin-2-one supplier is an individual or a company that provides 3-{[(5-nitro-2-furyl)methylene]amino}-1,3-oxazolidin-2-one active pharmaceutical ingredient (API) or 3-{[(5-nitro-2-furyl)methylene]amino}-1,3-oxazolidin-2-one finished formulations upon request. The 3-{[(5-nitro-2-furyl)methylene]amino}-1,3-oxazolidin-2-one suppliers may include 3-{[(5-nitro-2-furyl)methylene]amino}-1,3-oxazolidin-2-one API manufacturers, exporters, distributors and traders.
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A 3-{[(5-nitro-2-furyl)methylene]amino}-1,3-oxazolidin-2-one DMF (Drug Master File) is a document detailing the whole manufacturing process of 3-{[(5-nitro-2-furyl)methylene]amino}-1,3-oxazolidin-2-one active pharmaceutical ingredient (API) in detail. Different forms of 3-{[(5-nitro-2-furyl)methylene]amino}-1,3-oxazolidin-2-one DMFs exist exist since differing nations have different regulations, such as 3-{[(5-nitro-2-furyl)methylene]amino}-1,3-oxazolidin-2-one USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 3-{[(5-nitro-2-furyl)methylene]amino}-1,3-oxazolidin-2-one DMF submitted to regulatory agencies in the US is known as a USDMF. 3-{[(5-nitro-2-furyl)methylene]amino}-1,3-oxazolidin-2-one USDMF includes data on 3-{[(5-nitro-2-furyl)methylene]amino}-1,3-oxazolidin-2-one's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 3-{[(5-nitro-2-furyl)methylene]amino}-1,3-oxazolidin-2-one USDMF is kept confidential to protect the manufacturer’s intellectual property.
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We have 3 companies offering 3-{[(5-nitro-2-furyl)methylene]amino}-1,3-oxazolidin-2-one
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