Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Iberica S.L. Rubi ES
02 1CAMBREX KARLSKOGA AB Karlskoga SE
03 1CHEMINO PHARMA LIMITED Mumbai IN
04 1DELTA SYNTHETIC CO., LTD. New Taipei City TW
05 1HARMAN FINOCHEM LIMITED Mumbai IN
06 1MAHENDRA CHEMICALS Ahmedabad IN
07 1SOCIETÀ ITALIANA MEDICINALI SCANDICCI S.I.M.S. S.R.L Reggello IT
08 1SWATI SPENTOSE PVT. LTD. Mumbai IN
09 1VIWIT PHARMACEUTICAL CO. LTD Tengzhou CN
10 1W. R. GRACE & CO.-CONN. Columbia US
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Lidocaine Hydrochloride Monohydrate
Certificate Number : CEP 1996-020 - Rev 09
Status : Valid
Issue Date : 2024-05-29
Type : Chemical
Substance Number : 227
98
PharmaCompass offers a list of Lidocaine 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 Lidocaine Hydrochloride manufacturer or Lidocaine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lidocaine Hydrochloride manufacturer or Lidocaine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Lidocaine Hydrochloride API Price utilized in the formulation of products. Lidocaine Hydrochloride API Price is not always fixed or binding as the Lidocaine Hydrochloride Price is obtained through a variety of data sources. The Lidocaine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A LTA II KIT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LTA II KIT, including repackagers and relabelers. The FDA regulates LTA II KIT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LTA II KIT 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 LTA II KIT manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A LTA II KIT supplier is an individual or a company that provides LTA II KIT active pharmaceutical ingredient (API) or LTA II KIT finished formulations upon request. The LTA II KIT suppliers may include LTA II KIT API manufacturers, exporters, distributors and traders.
click here to find a list of LTA II KIT suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A LTA II KIT CEP of the European Pharmacopoeia monograph is often referred to as a LTA II KIT Certificate of Suitability (COS). The purpose of a LTA II KIT CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of LTA II KIT EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of LTA II KIT to their clients by showing that a LTA II KIT CEP has been issued for it. The manufacturer submits a LTA II KIT CEP (COS) as part of the market authorization procedure, and it takes on the role of a LTA II KIT CEP holder for the record. Additionally, the data presented in the LTA II KIT CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the LTA II KIT DMF.
A LTA II KIT CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. LTA II KIT 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 LTA II KIT suppliers with CEP (COS) on PharmaCompass.
We have 10 companies offering LTA II KIT
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