01 1Pfizer Inc
02 1SIGMA TAU
01 1CYCLOHEXIMIDE
02 1CYCLOHEXIMIDE (ACTIDIONE) U-4527
01 2U.S.A
01 2Inactive
01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2497
Submission : 1975-07-29
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2830
Submission : 1976-12-30
Status : Inactive
Type : II
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PharmaCompass offers a list of Cycloheximide 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 Cycloheximide manufacturer or Cycloheximide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cycloheximide manufacturer or Cycloheximide supplier.
PharmaCompass also assists you with knowing the Cycloheximide API Price utilized in the formulation of products. Cycloheximide API Price is not always fixed or binding as the Cycloheximide Price is obtained through a variety of data sources. The Cycloheximide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cycloheximide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cycloheximide, including repackagers and relabelers. The FDA regulates Cycloheximide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cycloheximide 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 Cycloheximide supplier is an individual or a company that provides Cycloheximide active pharmaceutical ingredient (API) or Cycloheximide finished formulations upon request. The Cycloheximide suppliers may include Cycloheximide API manufacturers, exporters, distributors and traders.
click here to find a list of Cycloheximide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cycloheximide DMF (Drug Master File) is a document detailing the whole manufacturing process of Cycloheximide active pharmaceutical ingredient (API) in detail. Different forms of Cycloheximide DMFs exist exist since differing nations have different regulations, such as Cycloheximide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cycloheximide DMF submitted to regulatory agencies in the US is known as a USDMF. Cycloheximide USDMF includes data on Cycloheximide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cycloheximide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cycloheximide suppliers with USDMF on PharmaCompass.
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