Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
01 1Cohance Lifesciences
02 1Apothecon Pharmaceuticals
03 1Cambrex Corporation
04 2Hetero Drugs
01 3MARAVIROC
02 1MARAVIROC (FORM-B)
03 1MARAVIROC AMORPHOUS
01 4India
02 1U.S.A
01 5Active
01 3Complete
02 2Blank
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
GDUFA
DMF Review : Complete
Rev. Date : 2021-12-20
Pay. Date : 2021-11-26
DMF Number : 35789
Submission : 2021-09-24
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2022-09-27
Pay. Date : 2022-08-10
DMF Number : 36917
Submission : 2022-03-30
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2021-03-02
Pay. Date : 2020-12-16
DMF Number : 34182
Submission : 2020-11-18
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25121
Submission : 2011-07-13
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25115
Submission : 2011-07-12
Status : Active
Type : II
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PharmaCompass offers a list of Maraviroc 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 Maraviroc manufacturer or Maraviroc supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Maraviroc manufacturer or Maraviroc supplier.
PharmaCompass also assists you with knowing the Maraviroc API Price utilized in the formulation of products. Maraviroc API Price is not always fixed or binding as the Maraviroc Price is obtained through a variety of data sources. The Maraviroc Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Selzentry manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Selzentry, including repackagers and relabelers. The FDA regulates Selzentry manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Selzentry 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 Selzentry manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Selzentry supplier is an individual or a company that provides Selzentry active pharmaceutical ingredient (API) or Selzentry finished formulations upon request. The Selzentry suppliers may include Selzentry API manufacturers, exporters, distributors and traders.
click here to find a list of Selzentry suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Selzentry DMF (Drug Master File) is a document detailing the whole manufacturing process of Selzentry active pharmaceutical ingredient (API) in detail. Different forms of Selzentry DMFs exist exist since differing nations have different regulations, such as Selzentry USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Selzentry DMF submitted to regulatory agencies in the US is known as a USDMF. Selzentry USDMF includes data on Selzentry's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Selzentry USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Selzentry suppliers with USDMF on PharmaCompass.
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