01 1Dishman Carbogen Amcis
01 1HEXETIDINE
01 1India
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24162
Submission : 2010-09-07
Status : Inactive
Type : II
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PharmaCompass offers a list of Hexetidine 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 Hexetidine manufacturer or Hexetidine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hexetidine manufacturer or Hexetidine supplier.
PharmaCompass also assists you with knowing the Hexetidine API Price utilized in the formulation of products. Hexetidine API Price is not always fixed or binding as the Hexetidine Price is obtained through a variety of data sources. The Hexetidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 38805A manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 38805A, including repackagers and relabelers. The FDA regulates 38805A manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 38805A API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of 38805A manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 38805A supplier is an individual or a company that provides 38805A active pharmaceutical ingredient (API) or 38805A finished formulations upon request. The 38805A suppliers may include 38805A API manufacturers, exporters, distributors and traders.
click here to find a list of 38805A suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 38805A DMF (Drug Master File) is a document detailing the whole manufacturing process of 38805A active pharmaceutical ingredient (API) in detail. Different forms of 38805A DMFs exist exist since differing nations have different regulations, such as 38805A USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 38805A DMF submitted to regulatory agencies in the US is known as a USDMF. 38805A USDMF includes data on 38805A's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 38805A USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 38805A suppliers with USDMF on PharmaCompass.
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