01 1PCAS Ecully FR
02 1SHANDONG BOYUAN PHARMACEUTICAL CO., LTD. Jinan City CN
03 1SYMED LABS LIMITED Hyderabad IN
04 1Shaanxi Hanjiang Pharmaceutical Group Co., Ltd. Hanzhong City CN
05 1TYCHE INDUSTRIES LIMITED Hyderabad IN
01 5Racecadotril
01 2China
02 1France
03 2India
01 5Valid
Certificate Number : R1-CEP 2014-373 - Rev 01
Status : Valid
Issue Date : 2021-08-06
Type : Chemical
Substance Number : 2171
Certificate Number : R1-CEP 2015-239 - Rev 01
Status : Valid
Issue Date : 2023-02-02
Type : Chemical
Substance Number : 2171
Certificate Number : CEP 2016-179 - Rev 01
Status : Valid
Issue Date : 2024-02-20
Type : Chemical
Substance Number : 2171
Certificate Number : R1-CEP 2015-249 - Rev 00
Status : Valid
Issue Date : 2021-07-09
Type : Chemical
Substance Number : 2171
Certificate Number : CEP 2013-223 - Rev 01
Status : Valid
Issue Date : 2024-04-12
Type : Chemical
Substance Number : 2171
87
PharmaCompass offers a list of Racecadotril 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 Racecadotril manufacturer or Racecadotril supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Racecadotril manufacturer or Racecadotril supplier.
PharmaCompass also assists you with knowing the Racecadotril API Price utilized in the formulation of products. Racecadotril API Price is not always fixed or binding as the Racecadotril Price is obtained through a variety of data sources. The Racecadotril Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A REDOTIL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of REDOTIL, including repackagers and relabelers. The FDA regulates REDOTIL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. REDOTIL 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 REDOTIL manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A REDOTIL supplier is an individual or a company that provides REDOTIL active pharmaceutical ingredient (API) or REDOTIL finished formulations upon request. The REDOTIL suppliers may include REDOTIL API manufacturers, exporters, distributors and traders.
click here to find a list of REDOTIL suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A REDOTIL CEP of the European Pharmacopoeia monograph is often referred to as a REDOTIL Certificate of Suitability (COS). The purpose of a REDOTIL CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of REDOTIL EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of REDOTIL to their clients by showing that a REDOTIL CEP has been issued for it. The manufacturer submits a REDOTIL CEP (COS) as part of the market authorization procedure, and it takes on the role of a REDOTIL CEP holder for the record. Additionally, the data presented in the REDOTIL CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the REDOTIL DMF.
A REDOTIL CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. REDOTIL 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 REDOTIL suppliers with CEP (COS) on PharmaCompass.
We have 5 companies offering REDOTIL
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