01 1Mitsubishi Tanabe Pharma
01 1L - TYROSINE ETHYLESTER MONOHYDROCHLORIDE
01 1Japan
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1831
Submission : 1971-12-17
Status : Inactive
Type : II
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PharmaCompass offers a list of L-Tyrosine Ethyl Ester 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 L-Tyrosine Ethyl Ester Hydrochloride manufacturer or L-Tyrosine Ethyl Ester Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the L-Tyrosine Ethyl Ester Hydrochloride API Price utilized in the formulation of products. L-Tyrosine Ethyl Ester Hydrochloride API Price is not always fixed or binding as the L-Tyrosine Ethyl Ester Hydrochloride Price is obtained through a variety of data sources. The L-Tyrosine Ethyl Ester Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A L-Tyrosine Ethyl Ester Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of L-Tyrosine Ethyl Ester Hydrochloride, including repackagers and relabelers. The FDA regulates L-Tyrosine Ethyl Ester Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. L-Tyrosine Ethyl Ester 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.
A L-Tyrosine Ethyl Ester Hydrochloride supplier is an individual or a company that provides L-Tyrosine Ethyl Ester Hydrochloride active pharmaceutical ingredient (API) or L-Tyrosine Ethyl Ester Hydrochloride finished formulations upon request. The L-Tyrosine Ethyl Ester Hydrochloride suppliers may include L-Tyrosine Ethyl Ester Hydrochloride API manufacturers, exporters, distributors and traders.
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A L-Tyrosine Ethyl Ester Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of L-Tyrosine Ethyl Ester Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of L-Tyrosine Ethyl Ester Hydrochloride DMFs exist exist since differing nations have different regulations, such as L-Tyrosine Ethyl Ester Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A L-Tyrosine Ethyl Ester Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. L-Tyrosine Ethyl Ester Hydrochloride USDMF includes data on L-Tyrosine Ethyl Ester Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The L-Tyrosine Ethyl Ester Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
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