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01 1ACIDCHEM INTERNATIONAL SDN BHD
02 1Subhash Chemical Industries
03 1Blank
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01 1HARIOL IPP (ISOPROPYL PALMITATE USP-NF)
02 1ISOPROPYL PALMITATE
03 1PROPAL (ISOPROPYL PALMITATE)
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01 1India
02 1Malaysia
03 1Blank
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01 2Active
02 1Inactive
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01 3Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18529
Submission : 2005-07-14
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 29296
Submission : 2015-04-15
Status : Active
Type : IV
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3838
Submission : 1980-06-16
Status : Inactive
Type : II
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PharmaCompass offers a list of Isopropyl Palmitate 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 Isopropyl Palmitate manufacturer or Isopropyl Palmitate supplier for your needs.
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PharmaCompass also assists you with knowing the Isopropyl Palmitate API Price utilized in the formulation of products. Isopropyl Palmitate API Price is not always fixed or binding as the Isopropyl Palmitate Price is obtained through a variety of data sources. The Isopropyl Palmitate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tox21_202558 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_202558, including repackagers and relabelers. The FDA regulates Tox21_202558 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_202558 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 Tox21_202558 supplier is an individual or a company that provides Tox21_202558 active pharmaceutical ingredient (API) or Tox21_202558 finished formulations upon request. The Tox21_202558 suppliers may include Tox21_202558 API manufacturers, exporters, distributors and traders.
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A Tox21_202558 DMF (Drug Master File) is a document detailing the whole manufacturing process of Tox21_202558 active pharmaceutical ingredient (API) in detail. Different forms of Tox21_202558 DMFs exist exist since differing nations have different regulations, such as Tox21_202558 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tox21_202558 DMF submitted to regulatory agencies in the US is known as a USDMF. Tox21_202558 USDMF includes data on Tox21_202558's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tox21_202558 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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