Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
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01 1Sanofi
02 1CHEMO IBERICA SA
03 1Fison
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01 2NEDOCROMIL SODIUM
02 1Nedocromil Disodium
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01 1France
02 1Spain
03 1United Kingdom
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01 3Inactive
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01 3Blank
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10944
Submission : 1994-06-17
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21169
Submission : 2007-12-19
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6513
Submission : 1986-07-30
Status : Inactive
Type : II
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PharmaCompass offers a list of Nedocromil Sodium 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 Nedocromil Sodium manufacturer or Nedocromil Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nedocromil Sodium manufacturer or Nedocromil Sodium supplier.
PharmaCompass also assists you with knowing the Nedocromil Sodium API Price utilized in the formulation of products. Nedocromil Sodium API Price is not always fixed or binding as the Nedocromil Sodium Price is obtained through a variety of data sources. The Nedocromil Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Rapitil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rapitil, including repackagers and relabelers. The FDA regulates Rapitil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rapitil 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 Rapitil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Rapitil supplier is an individual or a company that provides Rapitil active pharmaceutical ingredient (API) or Rapitil finished formulations upon request. The Rapitil suppliers may include Rapitil API manufacturers, exporters, distributors and traders.
click here to find a list of Rapitil suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Rapitil DMF (Drug Master File) is a document detailing the whole manufacturing process of Rapitil active pharmaceutical ingredient (API) in detail. Different forms of Rapitil DMFs exist exist since differing nations have different regulations, such as Rapitil USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Rapitil DMF submitted to regulatory agencies in the US is known as a USDMF. Rapitil USDMF includes data on Rapitil's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Rapitil USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Rapitil suppliers with USDMF on PharmaCompass.
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