01 1NOF CORPORATION
01 1[A-METHOXY-W-AMINOPROPYL, POLY (OXYETHYLENE)]-BLOCK-POLY (L-SODIUM GLUTAMATE)
01 1Japan
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 28196
Submission : 2014-04-10
Status : Inactive
Type : II
37
PharmaCompass offers a list of Sodium Glutamate 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 Sodium Glutamate manufacturer or Sodium Glutamate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Glutamate manufacturer or Sodium Glutamate supplier.
PharmaCompass also assists you with knowing the Sodium Glutamate API Price utilized in the formulation of products. Sodium Glutamate API Price is not always fixed or binding as the Sodium Glutamate Price is obtained through a variety of data sources. The Sodium Glutamate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Glutavene manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glutavene, including repackagers and relabelers. The FDA regulates Glutavene manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glutavene 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 Glutavene supplier is an individual or a company that provides Glutavene active pharmaceutical ingredient (API) or Glutavene finished formulations upon request. The Glutavene suppliers may include Glutavene API manufacturers, exporters, distributors and traders.
click here to find a list of Glutavene suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Glutavene DMF (Drug Master File) is a document detailing the whole manufacturing process of Glutavene active pharmaceutical ingredient (API) in detail. Different forms of Glutavene DMFs exist exist since differing nations have different regulations, such as Glutavene USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Glutavene DMF submitted to regulatory agencies in the US is known as a USDMF. Glutavene USDMF includes data on Glutavene's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Glutavene USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Glutavene suppliers with USDMF on PharmaCompass.
We have 1 companies offering Glutavene
Get in contact with the supplier of your choice:
