
Reset all filters
01 1DIVI'S LABORATORIES LIMITED Hyderabad IN
02 1HETERO DRUGS LIMITED Hyderabad IN
03 1IPCA Laboratories Limited Mumbai IN
04 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
Reset all filters
01 4Proguanil hydrochloride
Reset all filters
01 4India
Reset all filters
01 4Valid
Certificate Number : R1-CEP 2010-362 - Rev 02
Status : Valid
Issue Date : 2018-02-28
Type : Chemical
Substance Number : 2002
Certificate Number : R1-CEP 2011-182 - Rev 00
Status : Valid
Issue Date : 2018-08-20
Type : Chemical
Substance Number : 2002
Certificate Number : R1-CEP 2008-180 - Rev 03
Status : Valid
Issue Date : 2021-12-06
Type : Chemical
Substance Number : 2002
Certificate Number : CEP 2009-199 - Rev 04
Status : Valid
Issue Date : 2024-07-30
Type : Chemical
Substance Number : 2002
89
PharmaCompass offers a list of Proguanil 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 Proguanil manufacturer or Proguanil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Proguanil manufacturer or Proguanil supplier.
PharmaCompass also assists you with knowing the Proguanil API Price utilized in the formulation of products. Proguanil API Price is not always fixed or binding as the Proguanil Price is obtained through a variety of data sources. The Proguanil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A SN 12,837 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SN 12,837, including repackagers and relabelers. The FDA regulates SN 12,837 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SN 12,837 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 SN 12,837 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A SN 12,837 supplier is an individual or a company that provides SN 12,837 active pharmaceutical ingredient (API) or SN 12,837 finished formulations upon request. The SN 12,837 suppliers may include SN 12,837 API manufacturers, exporters, distributors and traders.
click here to find a list of SN 12,837 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A SN 12,837 CEP of the European Pharmacopoeia monograph is often referred to as a SN 12,837 Certificate of Suitability (COS). The purpose of a SN 12,837 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of SN 12,837 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of SN 12,837 to their clients by showing that a SN 12,837 CEP has been issued for it. The manufacturer submits a SN 12,837 CEP (COS) as part of the market authorization procedure, and it takes on the role of a SN 12,837 CEP holder for the record. Additionally, the data presented in the SN 12,837 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the SN 12,837 DMF.
A SN 12,837 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. SN 12,837 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 SN 12,837 suppliers with CEP (COS) on PharmaCompass.
We have 4 companies offering SN 12,837
Get in contact with the supplier of your choice: