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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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Propylhexedrine manufacturer or Propylhexedrine supplier.
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 Propylhexedrin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Propylhexedrin, including repackagers and relabelers. The FDA regulates Propylhexedrin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Propylhexedrin 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 Propylhexedrin supplier is an individual or a company that provides Propylhexedrin active pharmaceutical ingredient (API) or Propylhexedrin finished formulations upon request. The Propylhexedrin suppliers may include Propylhexedrin API manufacturers, exporters, distributors and traders.
click here to find a list of Propylhexedrin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Propylhexedrin DMF (Drug Master File) is a document detailing the whole manufacturing process of Propylhexedrin active pharmaceutical ingredient (API) in detail. Different forms of Propylhexedrin DMFs exist exist since differing nations have different regulations, such as Propylhexedrin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Propylhexedrin DMF submitted to regulatory agencies in the US is known as a USDMF. Propylhexedrin USDMF includes data on Propylhexedrin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Propylhexedrin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Propylhexedrin suppliers with USDMF on PharmaCompass.
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