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01 1Pfizer Inc
02 1SIGMA TAU
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01 1CYCLOHEXIMIDE
02 1CYCLOHEXIMIDE (ACTIDIONE) U-4527
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01 2U.S.A
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01 2Inactive
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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 Cicloheximida manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cicloheximida, including repackagers and relabelers. The FDA regulates Cicloheximida manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cicloheximida 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 Cicloheximida supplier is an individual or a company that provides Cicloheximida active pharmaceutical ingredient (API) or Cicloheximida finished formulations upon request. The Cicloheximida suppliers may include Cicloheximida API manufacturers, exporters, distributors and traders.
click here to find a list of Cicloheximida suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cicloheximida DMF (Drug Master File) is a document detailing the whole manufacturing process of Cicloheximida active pharmaceutical ingredient (API) in detail. Different forms of Cicloheximida DMFs exist exist since differing nations have different regulations, such as Cicloheximida USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cicloheximida DMF submitted to regulatory agencies in the US is known as a USDMF. Cicloheximida USDMF includes data on Cicloheximida's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cicloheximida USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cicloheximida suppliers with USDMF on PharmaCompass.
We have 2 companies offering Cicloheximida
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