01 1CTX LIFESCIENCES PVT. LIMITED Surat IN
02 1SIEGFRIED PHARMACHEMIKALIEN MINDEN GMBH Minden DE
01 2Oxymetazoline hydrochloride
01 1India
02 1Switzerland
01 2Valid
Certificate Number : R1-CEP 2008-324 - Rev 03
Status : Valid
Issue Date : 2018-05-18
Type : Chemical
Substance Number : 943
Certificate Number : R1-CEP 2008-064 - Rev 02
Status : Valid
Issue Date : 2021-01-15
Type : Chemical
Substance Number : 943
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PharmaCompass offers a list of Oxymetazoline 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 Oxymetazoline Hydrochloride manufacturer or Oxymetazoline Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxymetazoline Hydrochloride manufacturer or Oxymetazoline Hydrochloride supplier.
PharmaCompass also assists you with knowing the Oxymetazoline Hydrochloride API Price utilized in the formulation of products. Oxymetazoline Hydrochloride API Price is not always fixed or binding as the Oxymetazoline Hydrochloride Price is obtained through a variety of data sources. The Oxymetazoline Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Neo-Synephrine 12 Hour manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neo-Synephrine 12 Hour, including repackagers and relabelers. The FDA regulates Neo-Synephrine 12 Hour manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neo-Synephrine 12 Hour 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 Neo-Synephrine 12 Hour supplier is an individual or a company that provides Neo-Synephrine 12 Hour active pharmaceutical ingredient (API) or Neo-Synephrine 12 Hour finished formulations upon request. The Neo-Synephrine 12 Hour suppliers may include Neo-Synephrine 12 Hour API manufacturers, exporters, distributors and traders.
click here to find a list of Neo-Synephrine 12 Hour suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Neo-Synephrine 12 Hour CEP of the European Pharmacopoeia monograph is often referred to as a Neo-Synephrine 12 Hour Certificate of Suitability (COS). The purpose of a Neo-Synephrine 12 Hour CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Neo-Synephrine 12 Hour EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Neo-Synephrine 12 Hour to their clients by showing that a Neo-Synephrine 12 Hour CEP has been issued for it. The manufacturer submits a Neo-Synephrine 12 Hour CEP (COS) as part of the market authorization procedure, and it takes on the role of a Neo-Synephrine 12 Hour CEP holder for the record. Additionally, the data presented in the Neo-Synephrine 12 Hour CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Neo-Synephrine 12 Hour DMF.
A Neo-Synephrine 12 Hour CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Neo-Synephrine 12 Hour 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 Neo-Synephrine 12 Hour suppliers with CEP (COS) on PharmaCompass.
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