Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
01 1Evonik
02 1Ingredion Pharma Solutions
03 3Irvine Scientific Sales Company
04 1Roquette
05 1Shandong Tianli Pharmaceutical Co ltd
06 1Weifang Shengtai Pharmaceutical
07 2XIWANG PHARMACEUTICAL CO LTD
01 1ANHYDROUS DEXTROSE USP
02 1BIODEGRADABLE POLYMER EXCIPIENTS (GLUCOSE-INITIATED)
03 1C36 (GLUCOSE 5G/L) POWDER
04 3DEXTROSE ANHYDROUS
05 1DEXTROSE MONOHYDRATE
06 1DEXTROSE MONOHYDRATE, USP GRADE
07 1DME HIGH GLUCOSE-LIQUID # 9031
08 1DME HIGH GLUCOSE-LIQUID #9024
01 4China
02 1France
03 1Germany
04 4U.S.A
01 8Active
02 2Inactive
01 2Complete
02 8Blank
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36319
Submission : 2021-11-29
Status : Active
Type : IV
GDUFA
DMF Review : Complete
Rev. Date : 2014-08-13
Pay. Date : 2013-12-04
DMF Number : 14294
Submission : 1999-06-30
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 28948
Submission : 2014-12-22
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 27874
Submission : 2013-12-23
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 27858
Submission : 2013-12-23
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2015-11-23
Pay. Date : 2015-01-05
DMF Number : 11059
Submission : 1994-09-01
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 35737
Submission : 2021-05-14
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 30087
Submission : 2015-11-23
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26449
Submission : 2012-09-07
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26450
Submission : 2012-09-07
Status : Inactive
Type : II
A Anhydrous Dextrose manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Anhydrous Dextrose, including repackagers and relabelers. The FDA regulates Anhydrous Dextrose manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Anhydrous Dextrose 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 Anhydrous Dextrose manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Anhydrous Dextrose supplier is an individual or a company that provides Anhydrous Dextrose active pharmaceutical ingredient (API) or Anhydrous Dextrose finished formulations upon request. The Anhydrous Dextrose suppliers may include Anhydrous Dextrose API manufacturers, exporters, distributors and traders.
click here to find a list of Anhydrous Dextrose suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Anhydrous Dextrose DMF (Drug Master File) is a document detailing the whole manufacturing process of Anhydrous Dextrose active pharmaceutical ingredient (API) in detail. Different forms of Anhydrous Dextrose DMFs exist exist since differing nations have different regulations, such as Anhydrous Dextrose USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Anhydrous Dextrose DMF submitted to regulatory agencies in the US is known as a USDMF. Anhydrous Dextrose USDMF includes data on Anhydrous Dextrose's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Anhydrous Dextrose USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Anhydrous Dextrose suppliers with USDMF on PharmaCompass.
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