01 1Otsuka Chemical Co Ltd
01 1NADIFLOXACIN DRUG SUBSTANCE
01 1Japan
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12418
Submission : 1997-03-01
Status : Inactive
Type : II
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PharmaCompass offers a list of Nadifloxacin 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 Nadifloxacin manufacturer or Nadifloxacin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nadifloxacin manufacturer or Nadifloxacin supplier.
PharmaCompass also assists you with knowing the Nadifloxacin API Price utilized in the formulation of products. Nadifloxacin API Price is not always fixed or binding as the Nadifloxacin Price is obtained through a variety of data sources. The Nadifloxacin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A NDFX manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NDFX, including repackagers and relabelers. The FDA regulates NDFX manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NDFX 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 NDFX manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A NDFX supplier is an individual or a company that provides NDFX active pharmaceutical ingredient (API) or NDFX finished formulations upon request. The NDFX suppliers may include NDFX API manufacturers, exporters, distributors and traders.
click here to find a list of NDFX suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A NDFX DMF (Drug Master File) is a document detailing the whole manufacturing process of NDFX active pharmaceutical ingredient (API) in detail. Different forms of NDFX DMFs exist exist since differing nations have different regulations, such as NDFX USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A NDFX DMF submitted to regulatory agencies in the US is known as a USDMF. NDFX USDMF includes data on NDFX's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The NDFX USDMF is kept confidential to protect the manufacturer’s intellectual property.
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