01 1HAS Healthcare Advanced Synthesis
02 1SAFC
01 2MECHLORETHAMINE HYDROCHLORIDE
01 1Switzerland
02 1U.S.A
01 1Active
02 1Inactive
01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37687
Submission : 2023-04-14
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10103
Submission : 1993-02-22
Status : Inactive
Type : II
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PharmaCompass offers a list of Mechlorethamine 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 Mechlorethamine manufacturer or Mechlorethamine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mechlorethamine manufacturer or Mechlorethamine supplier.
PharmaCompass also assists you with knowing the Mechlorethamine API Price utilized in the formulation of products. Mechlorethamine API Price is not always fixed or binding as the Mechlorethamine Price is obtained through a variety of data sources. The Mechlorethamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Mustargen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mustargen, including repackagers and relabelers. The FDA regulates Mustargen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mustargen 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 Mustargen supplier is an individual or a company that provides Mustargen active pharmaceutical ingredient (API) or Mustargen finished formulations upon request. The Mustargen suppliers may include Mustargen API manufacturers, exporters, distributors and traders.
click here to find a list of Mustargen suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Mustargen DMF (Drug Master File) is a document detailing the whole manufacturing process of Mustargen active pharmaceutical ingredient (API) in detail. Different forms of Mustargen DMFs exist exist since differing nations have different regulations, such as Mustargen USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Mustargen DMF submitted to regulatory agencies in the US is known as a USDMF. Mustargen USDMF includes data on Mustargen's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Mustargen USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Mustargen suppliers with USDMF on PharmaCompass.
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