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Status : Withdrawn by Holder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Status : Withdrawn by Holder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 KALETRA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of KALETRA, including repackagers and relabelers. The FDA regulates KALETRA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. KALETRA 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 KALETRA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A KALETRA supplier is an individual or a company that provides KALETRA active pharmaceutical ingredient (API) or KALETRA finished formulations upon request. The KALETRA suppliers may include KALETRA API manufacturers, exporters, distributors and traders.
click here to find a list of KALETRA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A KALETRA CEP of the European Pharmacopoeia monograph is often referred to as a KALETRA Certificate of Suitability (COS). The purpose of a KALETRA CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of KALETRA EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of KALETRA to their clients by showing that a KALETRA CEP has been issued for it. The manufacturer submits a KALETRA CEP (COS) as part of the market authorization procedure, and it takes on the role of a KALETRA CEP holder for the record. Additionally, the data presented in the KALETRA CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the KALETRA DMF.
A KALETRA CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. KALETRA 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 KALETRA suppliers with CEP (COS) on PharmaCompass.
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