01 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
02 1CIPLA LIMITED Mumbai IN
03 1HETERO DRUGS LIMITED Hyderabad IN
04 1LAURUS LABS LIMITED Hyderabad IN
05 1LUPIN LIMITED Mumbai IN
06 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
01 6Lopinavir
01 6India
01 4Valid
02 2Withdrawn by Holder
Certificate Number : CEP 2018-071 - Rev 01
Status : Valid
Issue Date : 2024-02-20
Type : Chemical
Substance Number : 2615
Certificate Number : R0-CEP 2015-306 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2018-02-28
Type : Chemical
Substance Number : 2615
Certificate Number : R0-CEP 2020-396 - Rev 00
Status : Valid
Issue Date : 2022-10-28
Type : Chemical
Substance Number : 2615
Certificate Number : R0-CEP 2020-103 - Rev 01
Status : Valid
Issue Date : 2023-01-25
Type : Chemical
Substance Number : 2615
Certificate Number : R0-CEP 2016-128 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2017-03-31
Type : Chemical
Substance Number : 2615
Certificate Number : CEP 2013-011 - Rev 03
Status : Valid
Issue Date : 2024-07-23
Type : Chemical
Substance Number : 2615
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PharmaCompass offers a list of Lopinavir 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 Lopinavir manufacturer or Lopinavir supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lopinavir manufacturer or Lopinavir supplier.
PharmaCompass also assists you with knowing the Lopinavir API Price utilized in the formulation of products. Lopinavir API Price is not always fixed or binding as the Lopinavir Price is obtained through a variety of data sources. The Lopinavir Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Aluviran manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aluviran, including repackagers and relabelers. The FDA regulates Aluviran manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aluviran 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 Aluviran manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aluviran supplier is an individual or a company that provides Aluviran active pharmaceutical ingredient (API) or Aluviran finished formulations upon request. The Aluviran suppliers may include Aluviran API manufacturers, exporters, distributors and traders.
click here to find a list of Aluviran suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Aluviran CEP of the European Pharmacopoeia monograph is often referred to as a Aluviran Certificate of Suitability (COS). The purpose of a Aluviran CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Aluviran EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Aluviran to their clients by showing that a Aluviran CEP has been issued for it. The manufacturer submits a Aluviran CEP (COS) as part of the market authorization procedure, and it takes on the role of a Aluviran CEP holder for the record. Additionally, the data presented in the Aluviran CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Aluviran DMF.
A Aluviran CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Aluviran 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 Aluviran suppliers with CEP (COS) on PharmaCompass.
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