01 1Waitaki Biosciences
02 1Blank
01 2LINOLEIC ACID
01 1New Zealand
02 1Blank
01 2Inactive
01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6706
Submission : 1986-12-04
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9288
Submission : 1991-08-13
Status : Inactive
Type : II
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PharmaCompass offers a list of Linoleic Acid 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 Linoleic Acid manufacturer or Linoleic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Linoleic Acid manufacturer or Linoleic Acid supplier.
PharmaCompass also assists you with knowing the Linoleic Acid API Price utilized in the formulation of products. Linoleic Acid API Price is not always fixed or binding as the Linoleic Acid Price is obtained through a variety of data sources. The Linoleic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Linolate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Linolate, including repackagers and relabelers. The FDA regulates Linolate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Linolate 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 Linolate supplier is an individual or a company that provides Linolate active pharmaceutical ingredient (API) or Linolate finished formulations upon request. The Linolate suppliers may include Linolate API manufacturers, exporters, distributors and traders.
click here to find a list of Linolate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Linolate DMF (Drug Master File) is a document detailing the whole manufacturing process of Linolate active pharmaceutical ingredient (API) in detail. Different forms of Linolate DMFs exist exist since differing nations have different regulations, such as Linolate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Linolate DMF submitted to regulatory agencies in the US is known as a USDMF. Linolate USDMF includes data on Linolate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Linolate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Linolate suppliers with USDMF on PharmaCompass.
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