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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
29
PharmaCompass offers a list of Octylmethoxycinnamate 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 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.
PharmaCompass also assists you with knowing the Octylmethoxycinnamate API Price utilized in the formulation of products. Octylmethoxycinnamate API Price is not always fixed or binding as the Octylmethoxycinnamate Price is obtained through a variety of data sources. The Octylmethoxycinnamate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A escalol 557 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of escalol 557, including repackagers and relabelers. The FDA regulates escalol 557 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. escalol 557 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 escalol 557 supplier is an individual or a company that provides escalol 557 active pharmaceutical ingredient (API) or escalol 557 finished formulations upon request. The escalol 557 suppliers may include escalol 557 API manufacturers, exporters, distributors and traders.
click here to find a list of escalol 557 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A escalol 557 DMF (Drug Master File) is a document detailing the whole manufacturing process of escalol 557 active pharmaceutical ingredient (API) in detail. Different forms of escalol 557 DMFs exist exist since differing nations have different regulations, such as escalol 557 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A escalol 557 DMF submitted to regulatory agencies in the US is known as a USDMF. escalol 557 USDMF includes data on escalol 557's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The escalol 557 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of escalol 557 suppliers with USDMF on PharmaCompass.
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