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01 2AMINO GMBH Frellstedt DE
02 1Ajinomoto Co., Inc. Tokyo JP
03 1Nippon Rika Co., Ltd. Tokyo JP
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01 3Tyrosine
02 1Tyrosine, Derived from fermentation
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01 2Germany
02 2Japan
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01 4Valid
Certificate Number : CEP 1999-023 - Rev 03
Status : Valid
Issue Date : 2024-02-14
Type : Chemical
Substance Number : 1161
Tyrosine, Derived From Fermentation
Certificate Number : R1-CEP 2016-157 - Rev 00
Status : Valid
Issue Date : 2023-01-12
Type : Chemical
Substance Number : 1161
Certificate Number : R1-CEP 1998-034 - Rev 02
Status : Valid
Issue Date : 2014-08-12
Type : Chemical
Substance Number : 1161
Certificate Number : R1-CEP 2002-192 - Rev 03
Status : Valid
Issue Date : 2014-10-03
Type : Chemical
Substance Number : 1161
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PharmaCompass offers a list of L-Tyrosine API 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 API manufacturer or L-Tyrosine API supplier for your needs.
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PharmaCompass also assists you with knowing the L-Tyrosine API API Price utilized in the formulation of products. L-Tyrosine API API Price is not always fixed or binding as the L-Tyrosine API Price is obtained through a variety of data sources. The L-Tyrosine API Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DSSTox_CID_3730 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_CID_3730, including repackagers and relabelers. The FDA regulates DSSTox_CID_3730 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_CID_3730 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 DSSTox_CID_3730 supplier is an individual or a company that provides DSSTox_CID_3730 active pharmaceutical ingredient (API) or DSSTox_CID_3730 finished formulations upon request. The DSSTox_CID_3730 suppliers may include DSSTox_CID_3730 API manufacturers, exporters, distributors and traders.
click here to find a list of DSSTox_CID_3730 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DSSTox_CID_3730 CEP of the European Pharmacopoeia monograph is often referred to as a DSSTox_CID_3730 Certificate of Suitability (COS). The purpose of a DSSTox_CID_3730 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of DSSTox_CID_3730 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of DSSTox_CID_3730 to their clients by showing that a DSSTox_CID_3730 CEP has been issued for it. The manufacturer submits a DSSTox_CID_3730 CEP (COS) as part of the market authorization procedure, and it takes on the role of a DSSTox_CID_3730 CEP holder for the record. Additionally, the data presented in the DSSTox_CID_3730 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the DSSTox_CID_3730 DMF.
A DSSTox_CID_3730 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. DSSTox_CID_3730 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of DSSTox_CID_3730 suppliers with CEP (COS) on PharmaCompass.
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