01 1IPCA Laboratories Limited Mumbai IN
02 1Unichem Laboratories Limited Mumbai IN
01 2Bendroflumethiazide
01 2India
01 2Valid
Certificate Number : R1-CEP 2007-142 - Rev 03
Status : Valid
Issue Date : 2018-04-23
Type : Chemical
Substance Number : 370
Certificate Number : CEP 2002-102 - Rev 02
Status : Valid
Issue Date : 2024-11-05
Type : Chemical
Substance Number : 370
50
PharmaCompass offers a list of Bendroflumethiazide 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 Bendroflumethiazide manufacturer or Bendroflumethiazide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Bendroflumethiazide manufacturer or Bendroflumethiazide supplier.
PharmaCompass also assists you with knowing the Bendroflumethiazide API Price utilized in the formulation of products. Bendroflumethiazide API Price is not always fixed or binding as the Bendroflumethiazide Price is obtained through a variety of data sources. The Bendroflumethiazide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Urizid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Urizid, including repackagers and relabelers. The FDA regulates Urizid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Urizid 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 Urizid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Urizid supplier is an individual or a company that provides Urizid active pharmaceutical ingredient (API) or Urizid finished formulations upon request. The Urizid suppliers may include Urizid API manufacturers, exporters, distributors and traders.
click here to find a list of Urizid suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Urizid CEP of the European Pharmacopoeia monograph is often referred to as a Urizid Certificate of Suitability (COS). The purpose of a Urizid CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Urizid EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Urizid to their clients by showing that a Urizid CEP has been issued for it. The manufacturer submits a Urizid CEP (COS) as part of the market authorization procedure, and it takes on the role of a Urizid CEP holder for the record. Additionally, the data presented in the Urizid CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Urizid DMF.
A Urizid CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Urizid 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 Urizid suppliers with CEP (COS) on PharmaCompass.
We have 2 companies offering Urizid
Get in contact with the supplier of your choice:
