01 CHENGDA PHARMACEUTICALS CO., LTD. Jiashan CN (1)
02 NORTHEAST PHARMACEUTICAL GROUP COMPANY, LIMITED Shenyang CN (1)
03 PHARMARESOURCES (KAIYUAN) COMPANY LIMITED Kaiyuan City CN (1)
01 Levocarnitine (3)
01 China (3)
01 Valid (2)
02 Withdrawn by Holder (1)
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PharmaCompass offers a list of Levocarnitine 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 Levocarnitine manufacturer or Levocarnitine supplier for your needs.
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PharmaCompass also assists you with knowing the Levocarnitine API Price utilized in the formulation of products. Levocarnitine API Price is not always fixed or binding as the Levocarnitine Price is obtained through a variety of data sources. The Levocarnitine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MolPort-001-760-007 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-760-007, including repackagers and relabelers. The FDA regulates MolPort-001-760-007 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-760-007 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 MolPort-001-760-007 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A MolPort-001-760-007 supplier is an individual or a company that provides MolPort-001-760-007 active pharmaceutical ingredient (API) or MolPort-001-760-007 finished formulations upon request. The MolPort-001-760-007 suppliers may include MolPort-001-760-007 API manufacturers, exporters, distributors and traders.
click here to find a list of MolPort-001-760-007 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A MolPort-001-760-007 CEP of the European Pharmacopoeia monograph is often referred to as a MolPort-001-760-007 Certificate of Suitability (COS). The purpose of a MolPort-001-760-007 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of MolPort-001-760-007 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of MolPort-001-760-007 to their clients by showing that a MolPort-001-760-007 CEP has been issued for it. The manufacturer submits a MolPort-001-760-007 CEP (COS) as part of the market authorization procedure, and it takes on the role of a MolPort-001-760-007 CEP holder for the record. Additionally, the data presented in the MolPort-001-760-007 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the MolPort-001-760-007 DMF.
A MolPort-001-760-007 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. MolPort-001-760-007 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 MolPort-001-760-007 suppliers with CEP (COS) on PharmaCompass.
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