Fareva: One stop for innovative drug development, precision manufacturing and high-quality APIs.
01 1Fareva
02 1Aurobindo Pharma Limited
03 1CHANGZHOU KONY PHARMACEUTICAL CO., LTD. CN 213 105 Changzhou
04 1Charioteer
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
Fareva: One stop for innovative drug development, precision manufacturing and high-quality APIs.
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 : 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 : 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
16
PharmaCompass offers a list of Ganciclovir API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Ganciclovir manufacturer or Ganciclovir supplier for your needs.
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A Vitrasert manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vitrasert, including repackagers and relabelers. The FDA regulates Vitrasert manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vitrasert 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 Vitrasert manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Vitrasert supplier is an individual or a company that provides Vitrasert active pharmaceutical ingredient (API) or Vitrasert finished formulations upon request. The Vitrasert suppliers may include Vitrasert API manufacturers, exporters, distributors and traders.
click here to find a list of Vitrasert suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Vitrasert DMF (Drug Master File) is a document detailing the whole manufacturing process of Vitrasert active pharmaceutical ingredient (API) in detail. Different forms of Vitrasert DMFs exist exist since differing nations have different regulations, such as Vitrasert USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Vitrasert DMF submitted to regulatory agencies in the US is known as a USDMF. Vitrasert USDMF includes data on Vitrasert's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Vitrasert USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Vitrasert suppliers with USDMF on PharmaCompass.
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