01 R L FINE CHEM PVT. LTD. Gowribidanur IN (2)
02 SIGMA-ALDRICH IRELAND LTD Arklow IE (1)
03 Union Quimico Farmaceutica, S.A. (Uquifa S.A.) Barcelona ES (1)
01 Doxylamine hydrogen succinate (3)
02 Doxylamine hydrogen succinate, Grade II (1)
01 India (2)
02 Spain (1)
03 U.S.A (1)
01 Valid (4)
44
PharmaCompass offers a list of Doxylamine Succinate 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 Doxylamine Succinate manufacturer or Doxylamine Succinate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Doxylamine Succinate manufacturer or Doxylamine Succinate supplier.
PharmaCompass also assists you with knowing the Doxylamine Succinate API Price utilized in the formulation of products. Doxylamine Succinate API Price is not always fixed or binding as the Doxylamine Succinate Price is obtained through a variety of data sources. The Doxylamine Succinate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DICLEGIS manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DICLEGIS, including repackagers and relabelers. The FDA regulates DICLEGIS manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DICLEGIS 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 DICLEGIS manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DICLEGIS supplier is an individual or a company that provides DICLEGIS active pharmaceutical ingredient (API) or DICLEGIS finished formulations upon request. The DICLEGIS suppliers may include DICLEGIS API manufacturers, exporters, distributors and traders.
click here to find a list of DICLEGIS suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DICLEGIS CEP of the European Pharmacopoeia monograph is often referred to as a DICLEGIS Certificate of Suitability (COS). The purpose of a DICLEGIS CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of DICLEGIS EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of DICLEGIS to their clients by showing that a DICLEGIS CEP has been issued for it. The manufacturer submits a DICLEGIS CEP (COS) as part of the market authorization procedure, and it takes on the role of a DICLEGIS CEP holder for the record. Additionally, the data presented in the DICLEGIS CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the DICLEGIS DMF.
A DICLEGIS CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. DICLEGIS 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 DICLEGIS suppliers with CEP (COS) on PharmaCompass.
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