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01 1Schütz & Co GmbH & Co DE 20095 Hamburg
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01 1TRIPELENNAMINE HYDROCHLORIDE
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01 1Germany
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01 1Inactive
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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 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 Pyristine (pristina) hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pyristine (pristina) hydrochloride, including repackagers and relabelers. The FDA regulates Pyristine (pristina) hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pyristine (pristina) hydrochloride 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 Pyristine (pristina) hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pyristine (pristina) hydrochloride supplier is an individual or a company that provides Pyristine (pristina) hydrochloride active pharmaceutical ingredient (API) or Pyristine (pristina) hydrochloride finished formulations upon request. The Pyristine (pristina) hydrochloride suppliers may include Pyristine (pristina) hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Pyristine (pristina) hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Pyristine (pristina) hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Pyristine (pristina) hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Pyristine (pristina) hydrochloride DMFs exist exist since differing nations have different regulations, such as Pyristine (pristina) hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Pyristine (pristina) hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Pyristine (pristina) hydrochloride USDMF includes data on Pyristine (pristina) hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Pyristine (pristina) hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
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