01 1CHINESE PEPTIDE COMPANY Hangzhou CN
02 1HYBIO PHARMACEUTICAL CO., LTD. Shenzhen CN
03 1PIRAMAL PHARMA LIMITED Mumbai IN
04 1PolyPeptide Laboratories (Sweden) AB Limhamn SE
01 4Terlipressin
01 2China
02 2U.S.A
01 4Valid
Certificate Number : R0-CEP 2020-111 - Rev 00
Status : Valid
Issue Date : 2022-05-23
Type : Chemical
Substance Number : 2646
Certificate Number : R0-CEP 2020-319 - Rev 00
Status : Valid
Issue Date : 2021-10-28
Type : Chemical
Substance Number : 2646
Certificate Number : R0-CEP 2021-470 - Rev 00
Status : Valid
Issue Date : 2022-12-06
Type : Chemical
Substance Number : 2646
Certificate Number : R0-CEP 2019-316 - Rev 00
Status : Valid
Issue Date : 2021-05-21
Type : Chemical
Substance Number : 2646
A Terlipressin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Terlipressin, including repackagers and relabelers. The FDA regulates Terlipressin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Terlipressin 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 Terlipressin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Terlipressin supplier is an individual or a company that provides Terlipressin active pharmaceutical ingredient (API) or Terlipressin finished formulations upon request. The Terlipressin suppliers may include Terlipressin API manufacturers, exporters, distributors and traders.
click here to find a list of Terlipressin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Terlipressin CEP of the European Pharmacopoeia monograph is often referred to as a Terlipressin Certificate of Suitability (COS). The purpose of a Terlipressin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Terlipressin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Terlipressin to their clients by showing that a Terlipressin CEP has been issued for it. The manufacturer submits a Terlipressin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Terlipressin CEP holder for the record. Additionally, the data presented in the Terlipressin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Terlipressin DMF.
A Terlipressin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Terlipressin 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 Terlipressin suppliers with CEP (COS) on PharmaCompass.
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