01 1Finar
01 1LAURYL LACTATE HP
01 1India
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31766
Submission : 2017-05-23
Status : Active
Type : IV
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PharmaCompass offers a list of Cyclochem Lvl 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 Cyclochem Lvl manufacturer or Cyclochem Lvl supplier for your needs.
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A Eutanol G manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eutanol G, including repackagers and relabelers. The FDA regulates Eutanol G manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eutanol G 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 Eutanol G supplier is an individual or a company that provides Eutanol G active pharmaceutical ingredient (API) or Eutanol G finished formulations upon request. The Eutanol G suppliers may include Eutanol G API manufacturers, exporters, distributors and traders.
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A Eutanol G DMF (Drug Master File) is a document detailing the whole manufacturing process of Eutanol G active pharmaceutical ingredient (API) in detail. Different forms of Eutanol G DMFs exist exist since differing nations have different regulations, such as Eutanol G USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Eutanol G DMF submitted to regulatory agencies in the US is known as a USDMF. Eutanol G USDMF includes data on Eutanol G's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Eutanol G USDMF is kept confidential to protect the manufacturer’s intellectual property.
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