01 1FDC Limited Mumbai IN
02 1FLEMING LABORATORIES LIMITED Nawabpet Village IN
03 1HIKAL LIMITED Bangalore IN
04 1JANSSEN PHARMACEUTICA NV Beerse BE
05 1Shaanxi Hanjiang Pharmaceutical Group Co. Ltd Hanzhong City CN
06 1VASUDHA PHARMA CHEM LIMITED Hyderabad IN
01 6Cinnarizine
01 1Belgium
02 1China
03 4India
01 1Expired
02 5Valid
Certificate Number : CEP 2003-150 - Rev 04
Status : Valid
Issue Date : 2025-04-07
Type : Chemical
Substance Number : 816
Certificate Number : CEP 2015-019 - Rev 01
Status : Valid
Issue Date : 2025-05-07
Type : Chemical
Substance Number : 816
Certificate Number : R1-CEP 2004-271 - Rev 04
Status : Valid
Issue Date : 2022-09-07
Type : Chemical
Substance Number : 816
Certificate Number : R2-CEP 1994-016 - Rev 03
Status : Valid
Issue Date : 2011-10-27
Type : Chemical
Substance Number : 816
Certificate Number : R0-CEP 2001-130 - Rev 01
Status : Expired
Issue Date : 2004-12-03
Type : Chemical
Substance Number : 816
Certificate Number : R0-CEP 2019-080 - Rev 01
Status : Valid
Issue Date : 2023-02-03
Type : Chemical
Substance Number : 816
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PharmaCompass offers a list of Cinnarizine 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 Cinnarizine manufacturer or Cinnarizine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cinnarizine manufacturer or Cinnarizine supplier.
PharmaCompass also assists you with knowing the Cinnarizine API Price utilized in the formulation of products. Cinnarizine API Price is not always fixed or binding as the Cinnarizine Price is obtained through a variety of data sources. The Cinnarizine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Glanil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glanil, including repackagers and relabelers. The FDA regulates Glanil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glanil 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 Glanil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glanil supplier is an individual or a company that provides Glanil active pharmaceutical ingredient (API) or Glanil finished formulations upon request. The Glanil suppliers may include Glanil API manufacturers, exporters, distributors and traders.
click here to find a list of Glanil suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Glanil CEP of the European Pharmacopoeia monograph is often referred to as a Glanil Certificate of Suitability (COS). The purpose of a Glanil CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Glanil EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Glanil to their clients by showing that a Glanil CEP has been issued for it. The manufacturer submits a Glanil CEP (COS) as part of the market authorization procedure, and it takes on the role of a Glanil CEP holder for the record. Additionally, the data presented in the Glanil CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Glanil DMF.
A Glanil CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Glanil 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 Glanil suppliers with CEP (COS) on PharmaCompass.
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