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01 13-CHLORO-IMINODIBENZYL
02 3IMINODIBENZYL
01 1China
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01 4Inactive
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GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26801
Submission : 2013-01-04
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7606
Submission : 1988-07-28
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 : 1483
Submission : 1970-02-11
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 : 1426
Submission : 1969-09-07
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 Dibenzylamine 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 Dibenzylamine manufacturer or Dibenzylamine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dibenzylamine manufacturer or Dibenzylamine supplier.
PharmaCompass also assists you with knowing the Dibenzylamine API Price utilized in the formulation of products. Dibenzylamine API Price is not always fixed or binding as the Dibenzylamine Price is obtained through a variety of data sources. The Dibenzylamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tox21_202836 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_202836, including repackagers and relabelers. The FDA regulates Tox21_202836 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_202836 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 Tox21_202836 supplier is an individual or a company that provides Tox21_202836 active pharmaceutical ingredient (API) or Tox21_202836 finished formulations upon request. The Tox21_202836 suppliers may include Tox21_202836 API manufacturers, exporters, distributors and traders.
click here to find a list of Tox21_202836 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tox21_202836 DMF (Drug Master File) is a document detailing the whole manufacturing process of Tox21_202836 active pharmaceutical ingredient (API) in detail. Different forms of Tox21_202836 DMFs exist exist since differing nations have different regulations, such as Tox21_202836 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tox21_202836 DMF submitted to regulatory agencies in the US is known as a USDMF. Tox21_202836 USDMF includes data on Tox21_202836's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tox21_202836 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Tox21_202836 suppliers with USDMF on PharmaCompass.
We have 1 companies offering Tox21_202836
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