01 1Schütz & Co GmbH & Co DE 20095 Hamburg
01 1TRIPELENNAMINE HYDROCHLORIDE
01 1Germany
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10582
Submission : 1993-11-19
Status : Inactive
Type : II
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PharmaCompass offers a list of Tripelennamine Hydrochloride 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 Tripelennamine Hydrochloride manufacturer or Tripelennamine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tripelennamine Hydrochloride manufacturer or Tripelennamine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Tripelennamine Hydrochloride API Price utilized in the formulation of products. Tripelennamine Hydrochloride API Price is not always fixed or binding as the Tripelennamine Hydrochloride Price is obtained through a variety of data sources. The Tripelennamine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Azaron manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Azaron, including repackagers and relabelers. The FDA regulates Azaron manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Azaron 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 Azaron supplier is an individual or a company that provides Azaron active pharmaceutical ingredient (API) or Azaron finished formulations upon request. The Azaron suppliers may include Azaron API manufacturers, exporters, distributors and traders.
click here to find a list of Azaron suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Azaron DMF (Drug Master File) is a document detailing the whole manufacturing process of Azaron active pharmaceutical ingredient (API) in detail. Different forms of Azaron DMFs exist exist since differing nations have different regulations, such as Azaron USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Azaron DMF submitted to regulatory agencies in the US is known as a USDMF. Azaron USDMF includes data on Azaron's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Azaron USDMF is kept confidential to protect the manufacturer’s intellectual property.
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