ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.
01 1ChemWerth Inc
02 1AstraZeneca
03 1Aurobindo Pharma Limited
04 1Beijing Sciecure Pharmaceutical
05 1Chia Tai Tianqing Pharmaceutical Group
06 1Emcure Pharmaceuticals
07 1GLAND PHARMA LIMITED
08 1Lianyungang Runzhong Pharmaceutical Co Ltd
09 1Maithri Drugs
10 1Trifarma
01 3FOSCARNET SODIUM
02 1FOSCARNET SODIUM INTRAVENOUS SOLUTION
03 5FOSCARNET SODIUM USP
04 1FOSCARNET SODIUM, NON STERILE, BULK DRUG SUBSTANCE
01 2China
02 4India
03 1Italy
04 2U.S.A
05 1United Kingdom
01 8Active
02 2Inactive
01 7Complete
02 3Blank
ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.
GDUFA
DMF Review : Complete
Rev. Date : 2015-07-10
Pay. Date : 2015-02-05
DMF Number : 28996
Submission : 2015-01-30
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6036
Submission : 1985-10-02
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2020-08-12
Pay. Date : 2020-07-23
DMF Number : 35025
Submission : 2020-07-24
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2020-01-03
Pay. Date : 2019-08-27
DMF Number : 33288
Submission : 2019-08-05
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11385
Submission : 1995-03-15
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2019-07-31
Pay. Date : 2019-07-05
DMF Number : 32652
Submission : 2018-03-30
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2016-01-08
Pay. Date : 2015-09-28
DMF Number : 29814
Submission : 2015-09-28
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2015-05-20
Pay. Date : 2015-03-11
DMF Number : 29056
Submission : 2015-02-05
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34968
Submission : 2020-07-04
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-12-18
Pay. Date : 2013-09-12
DMF Number : 19085
Submission : 2006-01-04
Status : Active
Type : II
A Foscarnet Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Foscarnet Sodium, including repackagers and relabelers. The FDA regulates Foscarnet Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Foscarnet Sodium 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 Foscarnet Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Foscarnet Sodium supplier is an individual or a company that provides Foscarnet Sodium active pharmaceutical ingredient (API) or Foscarnet Sodium finished formulations upon request. The Foscarnet Sodium suppliers may include Foscarnet Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Foscarnet Sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Foscarnet Sodium DMF (Drug Master File) is a document detailing the whole manufacturing process of Foscarnet Sodium active pharmaceutical ingredient (API) in detail. Different forms of Foscarnet Sodium DMFs exist exist since differing nations have different regulations, such as Foscarnet Sodium USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Foscarnet Sodium DMF submitted to regulatory agencies in the US is known as a USDMF. Foscarnet Sodium USDMF includes data on Foscarnet Sodium's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Foscarnet Sodium USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Foscarnet Sodium suppliers with USDMF on PharmaCompass.
We have 10 companies offering Foscarnet Sodium
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