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01 1Lonza Group
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01 1PROPYLHEXEDRINE
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01 1Switzerland
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01 1Inactive
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01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10389
Submission : 1993-07-29
Status : Inactive
Type : II
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PharmaCompass offers a list of Propylhexedrine 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 Propylhexedrine manufacturer or Propylhexedrine supplier for your needs.
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PharmaCompass also assists you with knowing the Propylhexedrine API Price utilized in the formulation of products. Propylhexedrine API Price is not always fixed or binding as the Propylhexedrine Price is obtained through a variety of data sources. The Propylhexedrine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A (2-cyclohexyl-isopropyl)methylamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (2-cyclohexyl-isopropyl)methylamine, including repackagers and relabelers. The FDA regulates (2-cyclohexyl-isopropyl)methylamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (2-cyclohexyl-isopropyl)methylamine 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 (2-cyclohexyl-isopropyl)methylamine supplier is an individual or a company that provides (2-cyclohexyl-isopropyl)methylamine active pharmaceutical ingredient (API) or (2-cyclohexyl-isopropyl)methylamine finished formulations upon request. The (2-cyclohexyl-isopropyl)methylamine suppliers may include (2-cyclohexyl-isopropyl)methylamine API manufacturers, exporters, distributors and traders.
click here to find a list of (2-cyclohexyl-isopropyl)methylamine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A (2-cyclohexyl-isopropyl)methylamine DMF (Drug Master File) is a document detailing the whole manufacturing process of (2-cyclohexyl-isopropyl)methylamine active pharmaceutical ingredient (API) in detail. Different forms of (2-cyclohexyl-isopropyl)methylamine DMFs exist exist since differing nations have different regulations, such as (2-cyclohexyl-isopropyl)methylamine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A (2-cyclohexyl-isopropyl)methylamine DMF submitted to regulatory agencies in the US is known as a USDMF. (2-cyclohexyl-isopropyl)methylamine USDMF includes data on (2-cyclohexyl-isopropyl)methylamine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The (2-cyclohexyl-isopropyl)methylamine USDMF is kept confidential to protect the manufacturer’s intellectual property.
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