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01 2Bio-Rad Laboratories
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01 1MACRO-PREP 50 EPOXIDE, DISTILLED SIZED SUPPORT
02 1MP50 EPOXIDE, UNDISTILLED, SIZED
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01 2India
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01 2Inactive
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01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10876
Submission : 1994-04-07
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9804
Submission : 1992-08-06
Status : Inactive
Type : II
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PharmaCompass offers a list of Oxirane 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 Oxirane manufacturer or Oxirane supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxirane manufacturer or Oxirane supplier.
PharmaCompass also assists you with knowing the Oxirane API Price utilized in the formulation of products. Oxirane API Price is not always fixed or binding as the Oxirane Price is obtained through a variety of data sources. The Oxirane Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ETO manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ETO, including repackagers and relabelers. The FDA regulates ETO manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ETO 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 ETO supplier is an individual or a company that provides ETO active pharmaceutical ingredient (API) or ETO finished formulations upon request. The ETO suppliers may include ETO API manufacturers, exporters, distributors and traders.
click here to find a list of ETO suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A ETO DMF (Drug Master File) is a document detailing the whole manufacturing process of ETO active pharmaceutical ingredient (API) in detail. Different forms of ETO DMFs exist exist since differing nations have different regulations, such as ETO USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A ETO DMF submitted to regulatory agencies in the US is known as a USDMF. ETO USDMF includes data on ETO's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The ETO USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of ETO suppliers with USDMF on PharmaCompass.
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