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01 1Novo Nordisk
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01 1SUBTILISIN A
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01 1Denmark
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01 1Inactive
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01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8133
Submission : 1989-07-14
Status : Inactive
Type : II
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PharmaCompass offers a list of SUBTILISIN A SUBSTRATE I 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 SUBTILISIN A SUBSTRATE I manufacturer or SUBTILISIN A SUBSTRATE I supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred SUBTILISIN A SUBSTRATE I manufacturer or SUBTILISIN A SUBSTRATE I supplier.
PharmaCompass also assists you with knowing the SUBTILISIN A SUBSTRATE I API Price utilized in the formulation of products. SUBTILISIN A SUBSTRATE I API Price is not always fixed or binding as the SUBTILISIN A SUBSTRATE I Price is obtained through a variety of data sources. The SUBTILISIN A SUBSTRATE I Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A SUBTILISIN A manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SUBTILISIN A, including repackagers and relabelers. The FDA regulates SUBTILISIN A manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SUBTILISIN A 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 SUBTILISIN A supplier is an individual or a company that provides SUBTILISIN A active pharmaceutical ingredient (API) or SUBTILISIN A finished formulations upon request. The SUBTILISIN A suppliers may include SUBTILISIN A API manufacturers, exporters, distributors and traders.
click here to find a list of SUBTILISIN A suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A SUBTILISIN A DMF (Drug Master File) is a document detailing the whole manufacturing process of SUBTILISIN A active pharmaceutical ingredient (API) in detail. Different forms of SUBTILISIN A DMFs exist exist since differing nations have different regulations, such as SUBTILISIN A USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A SUBTILISIN A DMF submitted to regulatory agencies in the US is known as a USDMF. SUBTILISIN A USDMF includes data on SUBTILISIN A's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The SUBTILISIN A USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of SUBTILISIN A suppliers with USDMF on PharmaCompass.
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