01 1Amino Chemicals
02 1Aurobindo Pharma Limited
03 1Hetero Drugs
04 1Quimica Sintetica
05 1Sun Pharmaceutical Industries Limited
06 1Zhejiang Huahai Pharmaceutical
01 3FOSINOPRIL SODIUM
02 2FOSINOPRIL SODIUM USP
03 1FOSINOPRIL SODIUM USP (NON-STERILE BULK)
01 1China
02 3India
03 1Malta
04 1Spain
01 3Active
02 3Inactive
01 1Complete
02 5Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15326
Submission : 2001-02-28
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19711
Submission : 2006-08-17
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16008
Submission : 2002-06-11
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15934
Submission : 2002-04-11
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16321
Submission : 2002-12-17
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-02-06
Pay. Date : 2012-11-23
DMF Number : 17805
Submission : 2004-10-27
Status : Active
Type : II
51
PharmaCompass offers a list of Fosinopril 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 Fosinopril manufacturer or Fosinopril supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fosinopril manufacturer or Fosinopril supplier.
PharmaCompass also assists you with knowing the Fosinopril API Price utilized in the formulation of products. Fosinopril API Price is not always fixed or binding as the Fosinopril Price is obtained through a variety of data sources. The Fosinopril Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fositens manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fositens, including repackagers and relabelers. The FDA regulates Fositens manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fositens 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 Fositens manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fositens supplier is an individual or a company that provides Fositens active pharmaceutical ingredient (API) or Fositens finished formulations upon request. The Fositens suppliers may include Fositens API manufacturers, exporters, distributors and traders.
click here to find a list of Fositens suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Fositens DMF (Drug Master File) is a document detailing the whole manufacturing process of Fositens active pharmaceutical ingredient (API) in detail. Different forms of Fositens DMFs exist exist since differing nations have different regulations, such as Fositens USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Fositens DMF submitted to regulatory agencies in the US is known as a USDMF. Fositens USDMF includes data on Fositens's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Fositens USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Fositens suppliers with USDMF on PharmaCompass.
We have 6 companies offering Fositens
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