01 1IDT Australia Limited
01 1TIAZOFURIN
01 1Australia
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14422
Submission : 1999-09-30
Status : Inactive
Type : II
A Tiazofurin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tiazofurin, including repackagers and relabelers. The FDA regulates Tiazofurin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tiazofurin 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 Tiazofurin supplier is an individual or a company that provides Tiazofurin active pharmaceutical ingredient (API) or Tiazofurin finished formulations upon request. The Tiazofurin suppliers may include Tiazofurin API manufacturers, exporters, distributors and traders.
click here to find a list of Tiazofurin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tiazofurin DMF (Drug Master File) is a document detailing the whole manufacturing process of Tiazofurin active pharmaceutical ingredient (API) in detail. Different forms of Tiazofurin DMFs exist exist since differing nations have different regulations, such as Tiazofurin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tiazofurin DMF submitted to regulatory agencies in the US is known as a USDMF. Tiazofurin USDMF includes data on Tiazofurin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tiazofurin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Tiazofurin suppliers with USDMF on PharmaCompass.
We have 1 companies offering Tiazofurin
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?