01 1Gilead Sciences
02 1NAGASE Europa GmbH
03 1Blank
01 12',3',5' TRI-O-ACETYLURIDINE
02 12',3',5'-TRI-O-ACETYLURIDINE
03 1TRIACETYLURIDINE
01 1Germany
02 1U.S.A
03 1Blank
01 3Inactive
01 3Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9517
Submission : 1992-01-31
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11241
Submission : 1994-12-13
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16448
Submission : 2003-02-28
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
22
PharmaCompass offers a list of Triacetyluridine 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 Triacetyluridine manufacturer or Triacetyluridine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Triacetyluridine manufacturer or Triacetyluridine supplier.
PharmaCompass also assists you with knowing the Triacetyluridine API Price utilized in the formulation of products. Triacetyluridine API Price is not always fixed or binding as the Triacetyluridine Price is obtained through a variety of data sources. The Triacetyluridine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vistonuridine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vistonuridine, including repackagers and relabelers. The FDA regulates Vistonuridine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vistonuridine API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Vistonuridine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vistonuridine supplier is an individual or a company that provides Vistonuridine active pharmaceutical ingredient (API) or Vistonuridine finished formulations upon request. The Vistonuridine suppliers may include Vistonuridine API manufacturers, exporters, distributors and traders.
click here to find a list of Vistonuridine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Vistonuridine DMF (Drug Master File) is a document detailing the whole manufacturing process of Vistonuridine active pharmaceutical ingredient (API) in detail. Different forms of Vistonuridine DMFs exist exist since differing nations have different regulations, such as Vistonuridine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Vistonuridine DMF submitted to regulatory agencies in the US is known as a USDMF. Vistonuridine USDMF includes data on Vistonuridine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Vistonuridine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Vistonuridine suppliers with USDMF on PharmaCompass.
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