01 2Fison
02 1Pharmacosmos AS
03 1SAFC
04 4Blank
01 1DEXTRAN POWDER
02 1DEXTRAN SULFATE
03 1EX-CELL CD CHO (63206 MODIFIED) CHO SERUM-FREE MEDIUM, CHEMICALLY DEFINED, W/500 MG/L DEXTRAN SULFATE, W/O L-GLUTAMINE, W/O HYPOXANTINE
04 1LOW MOLECULAR DEXTRAN
05 1MANUFACTURE OF DEXTRAN 40 POWDER
06 1MANUFACTURE OF DEXTRAN 70 POWDER
07 1MANUFACTURING AND DESCRIPTION (DEXTRAN)
08 1RHEOMACRODEX
01 1Denmark
02 1U.S.A
03 2United Kingdom
04 4Blank
01 1Active
02 7Inactive
01 8Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1184
Submission : 1968-05-07
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1183
Submission : 1968-05-07
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19584
Submission : 2006-06-30
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23092
Submission : 2009-07-31
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9447
Submission : 1991-12-05
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2573
Submission : 1975-12-03
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 462
Submission : 1962-01-08
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 353
Submission : 1959-11-16
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
A Dextran 40 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dextran 40, including repackagers and relabelers. The FDA regulates Dextran 40 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dextran 40 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 Dextran 40 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dextran 40 supplier is an individual or a company that provides Dextran 40 active pharmaceutical ingredient (API) or Dextran 40 finished formulations upon request. The Dextran 40 suppliers may include Dextran 40 API manufacturers, exporters, distributors and traders.
click here to find a list of Dextran 40 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dextran 40 DMF (Drug Master File) is a document detailing the whole manufacturing process of Dextran 40 active pharmaceutical ingredient (API) in detail. Different forms of Dextran 40 DMFs exist exist since differing nations have different regulations, such as Dextran 40 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Dextran 40 DMF submitted to regulatory agencies in the US is known as a USDMF. Dextran 40 USDMF includes data on Dextran 40's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Dextran 40 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Dextran 40 suppliers with USDMF on PharmaCompass.
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