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01 1VIRUPAKSHA ORGANICS LIMITED Hyderabad IN
02 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
03 1CIPLA LIMITED Mumbai IN
04 1H. Lundbeck A/S Valby DK
05 2HETERO DRUGS LIMITED Hyderabad IN
06 1IPCA Laboratories Limited Mumbai IN
07 2JUBILANT PHARMOVA LIMITED Nanjangud IN
08 1NATCO PHARMA LIMITED Hyderabad IN
09 1SHODHANA LABORATORIES PRIVATE LIMITED Hyderabad IN
10 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
11 1WUXI JIDA PHARMACEUTICAL CO., LTD. Jiangyin CN
12 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
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01 12Citalopram hydrobromide
02 1Citalopram hydrobromide, CTP Process
03 1Citalopram hydrobromide, DGR process
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01 2China
02 1Denmark
03 11India
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01 14Valid
Certificate Number : R0-CEP 2021-437 - Rev 00
Status : Valid
Issue Date : 2023-08-29
Type : Chemical
Substance Number : 2288
Certificate Number : R1-CEP 2009-012 - Rev 01
Status : Valid
Issue Date : 2018-02-08
Type : Chemical
Substance Number : 2288
Certificate Number : R1-CEP 2010-222 - Rev 00
Status : Valid
Issue Date : 2017-01-27
Type : Chemical
Substance Number : 2288
Certificate Number : CEP 2009-248 - Rev 05
Status : Valid
Issue Date : 2025-02-17
Type : Chemical
Substance Number : 2288
Certificate Number : R1-CEP 2010-296 - Rev 00
Status : Valid
Issue Date : 2016-12-08
Type : Chemical
Substance Number : 2288
Citalopram Hydrobromide, DGR Process
Certificate Number : R1-CEP 2010-379 - Rev 02
Status : Valid
Issue Date : 2022-08-24
Type : Chemical
Substance Number : 2288
Certificate Number : R1-CEP 2009-175 - Rev 05
Status : Valid
Issue Date : 2023-07-10
Type : Chemical
Substance Number : 2288
Certificate Number : R1-CEP 2009-390 - Rev 01
Status : Valid
Issue Date : 2017-02-14
Type : Chemical
Substance Number : 2288
Certificate Number : R1-CEP 2010-228 - Rev 02
Status : Valid
Issue Date : 2022-10-05
Type : Chemical
Substance Number : 2288
Certificate Number : R1-CEP 2011-214 - Rev 00
Status : Valid
Issue Date : 2017-09-14
Type : Chemical
Substance Number : 2288
36
PharmaCompass offers a list of Citalopram Hydrobromide 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 Citalopram Hydrobromide manufacturer or Citalopram Hydrobromide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Citalopram Hydrobromide manufacturer or Citalopram Hydrobromide supplier.
PharmaCompass also assists you with knowing the Citalopram Hydrobromide API Price utilized in the formulation of products. Citalopram Hydrobromide API Price is not always fixed or binding as the Citalopram Hydrobromide Price is obtained through a variety of data sources. The Citalopram Hydrobromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cipramil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cipramil, including repackagers and relabelers. The FDA regulates Cipramil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cipramil 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 Cipramil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cipramil supplier is an individual or a company that provides Cipramil active pharmaceutical ingredient (API) or Cipramil finished formulations upon request. The Cipramil suppliers may include Cipramil API manufacturers, exporters, distributors and traders.
click here to find a list of Cipramil suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cipramil CEP of the European Pharmacopoeia monograph is often referred to as a Cipramil Certificate of Suitability (COS). The purpose of a Cipramil CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cipramil EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cipramil to their clients by showing that a Cipramil CEP has been issued for it. The manufacturer submits a Cipramil CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cipramil CEP holder for the record. Additionally, the data presented in the Cipramil CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cipramil DMF.
A Cipramil CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cipramil 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 Cipramil suppliers with CEP (COS) on PharmaCompass.
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