01 1Productos Quimicos Naturales
02 1Blank
01 1CALIUM STEARATE CONTAING SODIUM LAURYL SULFATE (CS-SLS)
02 1SODIUM-17 DIHYROEQUILIN SULFATE
01 1Mexico
02 1Blank
01 2Inactive
01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14005
Submission : 1999-03-01
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3544
Submission : 1979-05-22
Status : Inactive
Type : II
Portfolio PDF
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Website
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PharmaCompass offers a list of Sodium Lauryl Sulfate API 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 Sodium Lauryl Sulfate API manufacturer or Sodium Lauryl Sulfate API supplier for your needs.
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PharmaCompass also assists you with knowing the Sodium Lauryl Sulfate API API Price utilized in the formulation of products. Sodium Lauryl Sulfate API API Price is not always fixed or binding as the Sodium Lauryl Sulfate API Price is obtained through a variety of data sources. The Sodium Lauryl Sulfate API Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Stepanol me dry manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Stepanol me dry, including repackagers and relabelers. The FDA regulates Stepanol me dry manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Stepanol me dry API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Stepanol me dry supplier is an individual or a company that provides Stepanol me dry active pharmaceutical ingredient (API) or Stepanol me dry finished formulations upon request. The Stepanol me dry suppliers may include Stepanol me dry API manufacturers, exporters, distributors and traders.
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A Stepanol me dry DMF (Drug Master File) is a document detailing the whole manufacturing process of Stepanol me dry active pharmaceutical ingredient (API) in detail. Different forms of Stepanol me dry DMFs exist exist since differing nations have different regulations, such as Stepanol me dry USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Stepanol me dry DMF submitted to regulatory agencies in the US is known as a USDMF. Stepanol me dry USDMF includes data on Stepanol me dry's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Stepanol me dry USDMF is kept confidential to protect the manufacturer’s intellectual property.
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