Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
01 1BIOPHORE INDIA PHARMACEUTICALS PVT. LTD. Hyderabad IN
02 1LOBA BIOTECH GMBH Fischamend AT
03 1MICRO LABS LIMITED Bengaluru IN
01 3Naphazoline Hydrochloride
01 1Austria
02 2India
01 3Valid
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
Certificate Number : CEP 2022-117 - Rev 00
Status : Valid
Issue Date : 2023-11-27
Type : Chemical
Substance Number : 730
Certificate Number : CEP 2021-445 - Rev 01
Status : Valid
Issue Date : 2024-03-22
Type : Chemical
Substance Number : 730
Certificate Number : CEP 2019-188 - Rev 02
Status : Valid
Issue Date : 2024-09-30
Type : Chemical
Substance Number : 730
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PharmaCompass offers a list of Naphazoline 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 Naphazoline Hydrochloride manufacturer or Naphazoline Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Naphazoline Hydrochloride manufacturer or Naphazoline Hydrochloride supplier.
PharmaCompass also assists you with knowing the Naphazoline Hydrochloride API Price utilized in the formulation of products. Naphazoline Hydrochloride API Price is not always fixed or binding as the Naphazoline Hydrochloride Price is obtained through a variety of data sources. The Naphazoline Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sanorin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sanorin, including repackagers and relabelers. The FDA regulates Sanorin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sanorin 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 Sanorin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sanorin supplier is an individual or a company that provides Sanorin active pharmaceutical ingredient (API) or Sanorin finished formulations upon request. The Sanorin suppliers may include Sanorin API manufacturers, exporters, distributors and traders.
click here to find a list of Sanorin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sanorin CEP of the European Pharmacopoeia monograph is often referred to as a Sanorin Certificate of Suitability (COS). The purpose of a Sanorin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Sanorin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Sanorin to their clients by showing that a Sanorin CEP has been issued for it. The manufacturer submits a Sanorin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Sanorin CEP holder for the record. Additionally, the data presented in the Sanorin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Sanorin DMF.
A Sanorin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Sanorin 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 Sanorin suppliers with CEP (COS) on PharmaCompass.
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