01 1Nycomed Austria GmbH
01 1LORNOXICAM
01 1Austria
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16755
Submission : 2003-08-07
Status : Inactive
Type : II
A Lornoxicam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lornoxicam, including repackagers and relabelers. The FDA regulates Lornoxicam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lornoxicam 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 Lornoxicam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lornoxicam supplier is an individual or a company that provides Lornoxicam active pharmaceutical ingredient (API) or Lornoxicam finished formulations upon request. The Lornoxicam suppliers may include Lornoxicam API manufacturers, exporters, distributors and traders.
click here to find a list of Lornoxicam suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lornoxicam DMF (Drug Master File) is a document detailing the whole manufacturing process of Lornoxicam active pharmaceutical ingredient (API) in detail. Different forms of Lornoxicam DMFs exist exist since differing nations have different regulations, such as Lornoxicam USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Lornoxicam DMF submitted to regulatory agencies in the US is known as a USDMF. Lornoxicam USDMF includes data on Lornoxicam's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Lornoxicam USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Lornoxicam suppliers with USDMF on PharmaCompass.
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