01 1JUBILANT PHARMOVA LIMITED Nanjangud IN
02 3TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
01 1Citalopram hydrobromide, Process II
02 2Citalopram hydrochloride
03 1Citalopram hydrochloride, Process II
01 4India
01 4Valid
Certificate Number : R1-CEP 2009-205 - Rev 02
Status : Valid
Issue Date : 2022-08-24
Type : Chemical
Substance Number : 2203
Certificate Number : CEP 2010-007 - Rev 04
Status : Valid
Issue Date : 2024-07-29
Type : Chemical
Substance Number : 2203
Citalopram Hydrochloride, Process II
Certificate Number : CEP 2019-233 - Rev 01
Status : Valid
Issue Date : 2024-07-29
Type : Chemical
Substance Number : 2203
Citalopram Hydrobromide, Process II
Certificate Number : CEP 2021-462 - Rev 01
Status : Valid
Issue Date : 2024-07-30
Type : Chemical
Substance Number : 2288
A Citalopram Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Citalopram Hydrochloride, including repackagers and relabelers. The FDA regulates Citalopram Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Citalopram Hydrochloride 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 Citalopram Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Citalopram Hydrochloride supplier is an individual or a company that provides Citalopram Hydrochloride active pharmaceutical ingredient (API) or Citalopram Hydrochloride finished formulations upon request. The Citalopram Hydrochloride suppliers may include Citalopram Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Citalopram Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Citalopram Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Citalopram Hydrochloride Certificate of Suitability (COS). The purpose of a Citalopram Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Citalopram Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Citalopram Hydrochloride to their clients by showing that a Citalopram Hydrochloride CEP has been issued for it. The manufacturer submits a Citalopram Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Citalopram Hydrochloride CEP holder for the record. Additionally, the data presented in the Citalopram Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Citalopram Hydrochloride DMF.
A Citalopram Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Citalopram Hydrochloride 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 Citalopram Hydrochloride suppliers with CEP (COS) on PharmaCompass.
We have 2 companies offering Citalopram Hydrochloride
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
