Tagoor's product development expertise, backed by our comprehensive understanding of the processes, helps us offer high-quality APIs.
01 1TAGOOR LABORATORIES PRIVATE LIMITED Visakhapatnam IN
02 1ARENE LIFE SCIENCES PRIVATE LIMITED Ramachandrapuram IN
03 1CADILA PHARMACEUTICALS LIMITED Ankleshwar IN
04 1MATRIX PHARMACORP PRIVATE LIMITED Sangareddy District IN
05 1MOREPEN LABORATORIES LIMITED Baddi IN
06 1QUIMICA SINTETICA S.A. Alcala De Henares ES
07 1ROLABO OUTSOURCING, S.L. Zaragoza ES
08 1SCHERING-PLOUGH EUROPE Brussels BE
09 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
10 1VASUDHA PHARMA CHEM LIMITED Hyderabad IN
Tagoor's product development expertise, backed by our comprehensive understanding of the processes, helps us offer high-quality APIs.
Certificate Number : CEP 2023-059 - Rev 00
Status : Valid
Issue Date : 2024-07-30
Type : Chemical
Substance Number : 2124
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PharmaCompass offers a list of Loratadine 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 Loratadine manufacturer or Loratadine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Loratadine manufacturer or Loratadine supplier.
PharmaCompass also assists you with knowing the Loratadine API Price utilized in the formulation of products. Loratadine API Price is not always fixed or binding as the Loratadine Price is obtained through a variety of data sources. The Loratadine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Restamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Restamine, including repackagers and relabelers. The FDA regulates Restamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Restamine 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 Restamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Restamine supplier is an individual or a company that provides Restamine active pharmaceutical ingredient (API) or Restamine finished formulations upon request. The Restamine suppliers may include Restamine API manufacturers, exporters, distributors and traders.
click here to find a list of Restamine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Restamine CEP of the European Pharmacopoeia monograph is often referred to as a Restamine Certificate of Suitability (COS). The purpose of a Restamine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Restamine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Restamine to their clients by showing that a Restamine CEP has been issued for it. The manufacturer submits a Restamine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Restamine CEP holder for the record. Additionally, the data presented in the Restamine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Restamine DMF.
A Restamine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Restamine 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 Restamine suppliers with CEP (COS) on PharmaCompass.
We have 10 companies offering Restamine
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