With Virupaksha, you get a quality product with on-time delivery.
01 1VIRUPAKSHA ORGANICS LIMITED Hyderabad IN
02 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
03 1CIPLA LIMITED Mumbai IN
04 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
05 1H. Lundbeck A/S Valby DK
06 2HETERO DRUGS LIMITED Hyderabad IN
07 1IPCA Laboratories Limited Mumbai IN
08 2JUBILANT PHARMOVA LIMITED Nanjangud IN
09 1NATCO PHARMA LIMITED Hyderabad IN
10 1SHODHANA LABORATORIES PRIVATE LIMITED Hyderabad IN
11 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
12 1WUXI JIDA PHARMACEUTICAL CO., LTD. Jiangyin CN
13 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
With Virupaksha, you get a quality product with on-time delivery.
Certificate Number : R0-CEP 2021-437 - Rev 00
Status : Valid
Issue Date : 2023-08-29
Type : Chemical
Substance Number : 2288
98
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 Lupram manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lupram, including repackagers and relabelers. The FDA regulates Lupram manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lupram 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 Lupram manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lupram supplier is an individual or a company that provides Lupram active pharmaceutical ingredient (API) or Lupram finished formulations upon request. The Lupram suppliers may include Lupram API manufacturers, exporters, distributors and traders.
click here to find a list of Lupram suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lupram CEP of the European Pharmacopoeia monograph is often referred to as a Lupram Certificate of Suitability (COS). The purpose of a Lupram CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Lupram EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Lupram to their clients by showing that a Lupram CEP has been issued for it. The manufacturer submits a Lupram CEP (COS) as part of the market authorization procedure, and it takes on the role of a Lupram CEP holder for the record. Additionally, the data presented in the Lupram CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Lupram DMF.
A Lupram CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Lupram 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 Lupram suppliers with CEP (COS) on PharmaCompass.
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