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01 1Corden Pharma Bergamo S.p.A
02 1Blank
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01 1GUANETHIDINE MONOSULFATE
02 1GUANETHIDINE SULFATE, USP
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01 1Italy
02 1Blank
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01 2Inactive
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01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5122
Submission : 1983-08-26
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5070
Submission : 1983-07-26
Status : Inactive
Type : II
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PharmaCompass offers a list of Guanethidine 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 Guanethidine manufacturer or Guanethidine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Guanethidine manufacturer or Guanethidine supplier.
PharmaCompass also assists you with knowing the Guanethidine API Price utilized in the formulation of products. Guanethidine API Price is not always fixed or binding as the Guanethidine Price is obtained through a variety of data sources. The Guanethidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Oktadin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oktadin, including repackagers and relabelers. The FDA regulates Oktadin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oktadin 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 Oktadin supplier is an individual or a company that provides Oktadin active pharmaceutical ingredient (API) or Oktadin finished formulations upon request. The Oktadin suppliers may include Oktadin API manufacturers, exporters, distributors and traders.
click here to find a list of Oktadin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Oktadin DMF (Drug Master File) is a document detailing the whole manufacturing process of Oktadin active pharmaceutical ingredient (API) in detail. Different forms of Oktadin DMFs exist exist since differing nations have different regulations, such as Oktadin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Oktadin DMF submitted to regulatory agencies in the US is known as a USDMF. Oktadin USDMF includes data on Oktadin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Oktadin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Oktadin suppliers with USDMF on PharmaCompass.
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