01 1Cargill SLU
02 1Roquette
03 1Weifang Shengtai Pharmaceutical
01 1C* PHARMDEX 02010 (GLUCOSE MONOHYDRATE)
02 1DEXTROSE MONOHYDRATE
03 1DEXTROSE MONOHYDRATE USP GRADE (LYCADEX® PF)
01 1China
02 1France
03 1Spain
01 3Active
01 1Complete
02 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31910
Submission : 2017-11-07
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-05-01
Pay. Date : 2014-04-29
DMF Number : 4697
Submission : 1982-10-27
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 30079
Submission : 2015-11-23
Status : Active
Type : II
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PharmaCompass offers a list of Dextrose Monohydrate API 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 Dextrose Monohydrate API manufacturer or Dextrose Monohydrate API supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dextrose Monohydrate API manufacturer or Dextrose Monohydrate API supplier.
PharmaCompass also assists you with knowing the Dextrose Monohydrate API API Price utilized in the formulation of products. Dextrose Monohydrate API API Price is not always fixed or binding as the Dextrose Monohydrate API Price is obtained through a variety of data sources. The Dextrose Monohydrate API Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A C6H12O6.H2O manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C6H12O6.H2O, including repackagers and relabelers. The FDA regulates C6H12O6.H2O manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C6H12O6.H2O 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 C6H12O6.H2O supplier is an individual or a company that provides C6H12O6.H2O active pharmaceutical ingredient (API) or C6H12O6.H2O finished formulations upon request. The C6H12O6.H2O suppliers may include C6H12O6.H2O API manufacturers, exporters, distributors and traders.
click here to find a list of C6H12O6.H2O suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A C6H12O6.H2O DMF (Drug Master File) is a document detailing the whole manufacturing process of C6H12O6.H2O active pharmaceutical ingredient (API) in detail. Different forms of C6H12O6.H2O DMFs exist exist since differing nations have different regulations, such as C6H12O6.H2O USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A C6H12O6.H2O DMF submitted to regulatory agencies in the US is known as a USDMF. C6H12O6.H2O USDMF includes data on C6H12O6.H2O's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The C6H12O6.H2O USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of C6H12O6.H2O suppliers with USDMF on PharmaCompass.
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