01 1KUNSHAN ORIENTAL PHARMACEUTICAL CO LTD
02 1Recordati
01 2PHENYTOIN
01 1China
02 1Italy
01 2Active
01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20434
Submission : 2007-03-25
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23226
Submission : 2009-10-29
Status : Active
Type : II
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PharmaCompass offers a list of Phenytoin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Phenytoin manufacturer or Phenytoin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Phenytoin manufacturer or Phenytoin supplier.
A Neosidantoina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neosidantoina, including repackagers and relabelers. The FDA regulates Neosidantoina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neosidantoina 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 Neosidantoina manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Neosidantoina supplier is an individual or a company that provides Neosidantoina active pharmaceutical ingredient (API) or Neosidantoina finished formulations upon request. The Neosidantoina suppliers may include Neosidantoina API manufacturers, exporters, distributors and traders.
click here to find a list of Neosidantoina suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Neosidantoina DMF (Drug Master File) is a document detailing the whole manufacturing process of Neosidantoina active pharmaceutical ingredient (API) in detail. Different forms of Neosidantoina DMFs exist exist since differing nations have different regulations, such as Neosidantoina USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Neosidantoina DMF submitted to regulatory agencies in the US is known as a USDMF. Neosidantoina USDMF includes data on Neosidantoina's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Neosidantoina USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Neosidantoina suppliers with USDMF on PharmaCompass.
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