01 1Procos
01 1CHLOPHEDIANOL HYDROCHLORIDE
01 1Italy
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22902
Submission : 2009-06-25
Status : Active
Type : II
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PharmaCompass offers a list of Clofedanol 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 Clofedanol manufacturer or Clofedanol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clofedanol manufacturer or Clofedanol supplier.
PharmaCompass also assists you with knowing the Clofedanol API Price utilized in the formulation of products. Clofedanol API Price is not always fixed or binding as the Clofedanol Price is obtained through a variety of data sources. The Clofedanol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ulone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ulone, including repackagers and relabelers. The FDA regulates Ulone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ulone 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 Ulone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ulone supplier is an individual or a company that provides Ulone active pharmaceutical ingredient (API) or Ulone finished formulations upon request. The Ulone suppliers may include Ulone API manufacturers, exporters, distributors and traders.
click here to find a list of Ulone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ulone DMF (Drug Master File) is a document detailing the whole manufacturing process of Ulone active pharmaceutical ingredient (API) in detail. Different forms of Ulone DMFs exist exist since differing nations have different regulations, such as Ulone USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Ulone DMF submitted to regulatory agencies in the US is known as a USDMF. Ulone USDMF includes data on Ulone's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Ulone USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Ulone suppliers with USDMF on PharmaCompass.
