01 1MSN Laboratories
01 1LENVATINIB
01 1India
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33195
Submission : 2018-09-29
Status : Active
Type : II
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PharmaCompass offers a list of Lenvatinib 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 Lenvatinib manufacturer or Lenvatinib supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lenvatinib manufacturer or Lenvatinib supplier.
PharmaCompass also assists you with knowing the Lenvatinib API Price utilized in the formulation of products. Lenvatinib API Price is not always fixed or binding as the Lenvatinib Price is obtained through a variety of data sources. The Lenvatinib Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lenvima manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lenvima, including repackagers and relabelers. The FDA regulates Lenvima manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lenvima 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 Lenvima manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lenvima supplier is an individual or a company that provides Lenvima active pharmaceutical ingredient (API) or Lenvima finished formulations upon request. The Lenvima suppliers may include Lenvima API manufacturers, exporters, distributors and traders.
click here to find a list of Lenvima suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lenvima DMF (Drug Master File) is a document detailing the whole manufacturing process of Lenvima active pharmaceutical ingredient (API) in detail. Different forms of Lenvima DMFs exist exist since differing nations have different regulations, such as Lenvima USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Lenvima DMF submitted to regulatory agencies in the US is known as a USDMF. Lenvima USDMF includes data on Lenvima's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Lenvima USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Lenvima suppliers with USDMF on PharmaCompass.
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