01 1Tayca
01 1MICRO TITANIUM DIOXIDE MT-100TV DRUG SUBSTANCE
01 1Japan
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12195
Submission : 1996-10-31
Status : Inactive
Type : II
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A Tioxide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tioxide, including repackagers and relabelers. The FDA regulates Tioxide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tioxide 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 Tioxide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Tioxide supplier is an individual or a company that provides Tioxide active pharmaceutical ingredient (API) or Tioxide finished formulations upon request. The Tioxide suppliers may include Tioxide API manufacturers, exporters, distributors and traders.
click here to find a list of Tioxide suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Tioxide DMF (Drug Master File) is a document detailing the whole manufacturing process of Tioxide active pharmaceutical ingredient (API) in detail. Different forms of Tioxide DMFs exist exist since differing nations have different regulations, such as Tioxide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tioxide DMF submitted to regulatory agencies in the US is known as a USDMF. Tioxide USDMF includes data on Tioxide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tioxide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Tioxide suppliers with USDMF on PharmaCompass.
