Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1Sanofi
02 1ALP Pharm
03 1Changzhou Qianhong
04 1Dongying Tiandong Pharmaceutical Co., Ltd.
05 1GLAND PHARMA LIMITED
06 1HEBEI CHANGSHAN BIOCHEMICAL PHARMACEUTICAL CO., LTD.
07 1Leo Pharma
08 1Opocrin SpA
09 1Reliable Biopharmaceutical Corporation
10 1Shandong Chenzhong Biopharmaceutical Co.
01 3DALTEPARIN SODIUM
02 1DALTEPARIN SODIUM (DRUG SUBSTANCE, NON-STERILE)
03 1DALTEPARIN SODIUM BULK
04 1DALTEPARIN SODIUM PH.EUR.
05 1DALTEPARIN SODIUM USP
06 2NADROPARIN CALCIUM
07 1TINZAPARIN SODIUM DRUG SUBSTANCE
01 5China
02 1Denmark
03 1France
04 1India
05 1Italy
06 1U.S.A
01 3Active
02 7Inactive
01 1Complete
02 9Blank
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9939
Submission : 1992-11-02
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21950
Submission : 2008-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2018-02-22
Pay. Date : 2014-07-25
DMF Number : 20541
Submission : 2007-03-27
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20905
Submission : 2007-09-25
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25556
Submission : 2011-12-20
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 29154
Submission : 2015-03-06
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10596
Submission : 1993-12-07
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19658
Submission : 2006-08-04
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19038
Submission : 2005-12-15
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31703
Submission : 2017-04-21
Status : Active
Type : II
A Nadroparin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nadroparin, including repackagers and relabelers. The FDA regulates Nadroparin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nadroparin 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 Nadroparin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nadroparin supplier is an individual or a company that provides Nadroparin active pharmaceutical ingredient (API) or Nadroparin finished formulations upon request. The Nadroparin suppliers may include Nadroparin API manufacturers, exporters, distributors and traders.
click here to find a list of Nadroparin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Nadroparin DMF (Drug Master File) is a document detailing the whole manufacturing process of Nadroparin active pharmaceutical ingredient (API) in detail. Different forms of Nadroparin DMFs exist exist since differing nations have different regulations, such as Nadroparin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Nadroparin DMF submitted to regulatory agencies in the US is known as a USDMF. Nadroparin USDMF includes data on Nadroparin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Nadroparin USDMF is kept confidential to protect the manufacturer’s intellectual property.
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