01 1Galaxy Surfactants
02 2Blank
01 1OCTINOXATE
02 2PARSOL MCX
01 1India
02 2Blank
01 3Inactive
01 3Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26272
Submission : 2012-08-01
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7834
Submission : 1988-12-15
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7738
Submission : 1988-10-21
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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PharmaCompass offers a list of Octylmethoxycinnamate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Octylmethoxycinnamate manufacturer or Octylmethoxycinnamate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Octylmethoxycinnamate manufacturer or Octylmethoxycinnamate supplier.
A octinoxate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of octinoxate, including repackagers and relabelers. The FDA regulates octinoxate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. octinoxate 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 octinoxate supplier is an individual or a company that provides octinoxate active pharmaceutical ingredient (API) or octinoxate finished formulations upon request. The octinoxate suppliers may include octinoxate API manufacturers, exporters, distributors and traders.
click here to find a list of octinoxate suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A octinoxate DMF (Drug Master File) is a document detailing the whole manufacturing process of octinoxate active pharmaceutical ingredient (API) in detail. Different forms of octinoxate DMFs exist exist since differing nations have different regulations, such as octinoxate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A octinoxate DMF submitted to regulatory agencies in the US is known as a USDMF. octinoxate USDMF includes data on octinoxate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The octinoxate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of octinoxate suppliers with USDMF on PharmaCompass.
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