01 1Aurobindo Pharma Limited
02 1CHANGZHOU KONY PHARMACEUTICAL CO., LTD. CN 213 105 Changzhou
03 1Charioteer
04 1Fareva
05 1Sun Pharmaceutical Industries Limited
06 1Trifarma
01 3GANCICLOVIR
02 1GANCICLOVIR USP
03 1GANCICLOVIR USP (NON-STERILE API)
04 1GANCICLOVIR, USP
01 2China
02 2India
03 1Italy
04 1Luxembourg
01 4Active
02 2Inactive
01 3Complete
02 3Blank
GDUFA
DMF Review : Complete
Rev. Date : 2017-03-07
Pay. Date : 2017-02-15
DMF Number : 31402
Submission : 2017-02-18
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2016-06-02
Pay. Date : 2015-08-07
DMF Number : 28973
Submission : 2015-04-02
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 27133
Submission : 2013-05-02
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-01-30
Pay. Date : 2013-01-08
DMF Number : 15567
Submission : 2001-07-31
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16043
Submission : 2002-07-08
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23721
Submission : 2010-04-16
Status : Active
Type : II
17
PharmaCompass offers a list of Ganciclovir 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 Ganciclovir manufacturer or Ganciclovir supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ganciclovir manufacturer or Ganciclovir supplier.
PharmaCompass also assists you with knowing the Ganciclovir API Price utilized in the formulation of products. Ganciclovir API Price is not always fixed or binding as the Ganciclovir Price is obtained through a variety of data sources. The Ganciclovir Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cytovene manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cytovene, including repackagers and relabelers. The FDA regulates Cytovene manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cytovene 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 Cytovene manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cytovene supplier is an individual or a company that provides Cytovene active pharmaceutical ingredient (API) or Cytovene finished formulations upon request. The Cytovene suppliers may include Cytovene API manufacturers, exporters, distributors and traders.
click here to find a list of Cytovene suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cytovene DMF (Drug Master File) is a document detailing the whole manufacturing process of Cytovene active pharmaceutical ingredient (API) in detail. Different forms of Cytovene DMFs exist exist since differing nations have different regulations, such as Cytovene USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cytovene DMF submitted to regulatory agencies in the US is known as a USDMF. Cytovene USDMF includes data on Cytovene's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cytovene USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cytovene suppliers with USDMF on PharmaCompass.
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