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01 2Nippon Kayaku
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01 1DEOXYSPERGUALIN HYDROCHLORIDE
02 1DEOXYSPERGUALIN HYDROCHLORIDE FOR INJECTION
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01 2Japan
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01 2Inactive
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01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6533
Submission : 1986-08-12
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6537
Submission : 1986-08-12
Status : Inactive
Type : II
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PharmaCompass offers a list of Gusperimus 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 Gusperimus manufacturer or Gusperimus supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Gusperimus manufacturer or Gusperimus supplier.
PharmaCompass also assists you with knowing the Gusperimus API Price utilized in the formulation of products. Gusperimus API Price is not always fixed or binding as the Gusperimus Price is obtained through a variety of data sources. The Gusperimus Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Gusperimus manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gusperimus, including repackagers and relabelers. The FDA regulates Gusperimus manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gusperimus 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 Gusperimus supplier is an individual or a company that provides Gusperimus active pharmaceutical ingredient (API) or Gusperimus finished formulations upon request. The Gusperimus suppliers may include Gusperimus API manufacturers, exporters, distributors and traders.
click here to find a list of Gusperimus suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Gusperimus DMF (Drug Master File) is a document detailing the whole manufacturing process of Gusperimus active pharmaceutical ingredient (API) in detail. Different forms of Gusperimus DMFs exist exist since differing nations have different regulations, such as Gusperimus USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Gusperimus DMF submitted to regulatory agencies in the US is known as a USDMF. Gusperimus USDMF includes data on Gusperimus's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Gusperimus USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Gusperimus suppliers with USDMF on PharmaCompass.
We have 1 companies offering Gusperimus
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