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01 1HEXOBARBITAL, NF XIV
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USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2995
Submission : 1977-07-22
Status : Inactive
Type : II
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PharmaCompass offers a list of Hexobarbital 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 Hexobarbital manufacturer or Hexobarbital supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hexobarbital manufacturer or Hexobarbital supplier.
PharmaCompass also assists you with knowing the Hexobarbital API Price utilized in the formulation of products. Hexobarbital API Price is not always fixed or binding as the Hexobarbital Price is obtained through a variety of data sources. The Hexobarbital Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Citodon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Citodon, including repackagers and relabelers. The FDA regulates Citodon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Citodon 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 Citodon supplier is an individual or a company that provides Citodon active pharmaceutical ingredient (API) or Citodon finished formulations upon request. The Citodon suppliers may include Citodon API manufacturers, exporters, distributors and traders.
click here to find a list of Citodon suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Citodon DMF (Drug Master File) is a document detailing the whole manufacturing process of Citodon active pharmaceutical ingredient (API) in detail. Different forms of Citodon DMFs exist exist since differing nations have different regulations, such as Citodon USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Citodon DMF submitted to regulatory agencies in the US is known as a USDMF. Citodon USDMF includes data on Citodon's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Citodon USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Citodon suppliers with USDMF on PharmaCompass.