01 23M Company
02 23M Drug Delivery Systems
01 1R-848 DRUG SUBSTANCE AND DRUG PRODUCT (ORAL)
02 1R-848 ORAL DRUG PRODUCT
03 1RESIQUIMOD DRUG SUBSTANCE
04 1RESIQUIMOD TOPICAL GEL
01 4U.S.A
01 1Active
02 3Inactive
01 4Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14687
Submission : 2000-01-24
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13956
Submission : 1999-01-22
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24080
Submission : 2010-08-16
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24093
Submission : 2010-08-17
Status : Inactive
Type : II
13
PharmaCompass offers a list of Resiquimod 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 Resiquimod manufacturer or Resiquimod supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Resiquimod manufacturer or Resiquimod supplier.
PharmaCompass also assists you with knowing the Resiquimod API Price utilized in the formulation of products. Resiquimod API Price is not always fixed or binding as the Resiquimod Price is obtained through a variety of data sources. The Resiquimod Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A R848 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of R848, including repackagers and relabelers. The FDA regulates R848 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. R848 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A R848 supplier is an individual or a company that provides R848 active pharmaceutical ingredient (API) or R848 finished formulations upon request. The R848 suppliers may include R848 API manufacturers, exporters, distributors and traders.
click here to find a list of R848 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A R848 DMF (Drug Master File) is a document detailing the whole manufacturing process of R848 active pharmaceutical ingredient (API) in detail. Different forms of R848 DMFs exist exist since differing nations have different regulations, such as R848 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A R848 DMF submitted to regulatory agencies in the US is known as a USDMF. R848 USDMF includes data on R848's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The R848 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of R848 suppliers with USDMF on PharmaCompass.
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