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 1MOREPEN LABORATORIES LIMITED Baddi IN
05 1QUIMICA SINTETICA S.A. Alcala De Henares ES
06 1ROLABO OUTSOURCING, S.L. Zaragoza ES
07 1SCHERING-PLOUGH EUROPE Brussels BE
08 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
09 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
10 1VASUDHA PHARMA CHEM LIMITED Hyderabad IN
11 1ZYDUS LIFESCIENCES LIMITED Vadodara 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 KS-1079 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of KS-1079, including repackagers and relabelers. The FDA regulates KS-1079 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. KS-1079 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 KS-1079 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A KS-1079 supplier is an individual or a company that provides KS-1079 active pharmaceutical ingredient (API) or KS-1079 finished formulations upon request. The KS-1079 suppliers may include KS-1079 API manufacturers, exporters, distributors and traders.
click here to find a list of KS-1079 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A KS-1079 CEP of the European Pharmacopoeia monograph is often referred to as a KS-1079 Certificate of Suitability (COS). The purpose of a KS-1079 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of KS-1079 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of KS-1079 to their clients by showing that a KS-1079 CEP has been issued for it. The manufacturer submits a KS-1079 CEP (COS) as part of the market authorization procedure, and it takes on the role of a KS-1079 CEP holder for the record. Additionally, the data presented in the KS-1079 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the KS-1079 DMF.
A KS-1079 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. KS-1079 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 KS-1079 suppliers with CEP (COS) on PharmaCompass.
We have 11 companies offering KS-1079
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