01 1ALEMBIC LIMITED Vadodara IN
02 1Artemis Biotech Limited Hyderabad IN
03 2BIOCON LIMITED Bangalore IN
04 1CONCORD BIOTECH LIMITED Ahmedabad IN
05 1Henan Topfond Pharmaceutical Co., Ltd. Zhumadian CN
06 1KREBS BIOCHEMICALS & INDUSTRIES LIMITED Kothapalli IN
07 1KRKA, d.d., Novo mesto Novo mesto SI
08 1LEK PHARMACEUTICALS D.D. Ljubljana SI
09 1STERLING BIOTECH LIMITED Masar Village IN
10 1TAPI NL B.V. Amsterdam NL
11 1Zhejiang Hisun Pharmaceutical Co., Ltd. Taizhou City CN
01 12Lovastatin
01 2China
02 7India
03 2Slovenia
04 1Blank
01 5Valid
02 7Withdrawn by Holder
Certificate Number : R0-CEP 2014-083 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2015-11-13
Type : Chemical
Substance Number : 1538
Certificate Number : R0-CEP 2003-269 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2006-08-03
Type : Chemical
Substance Number : 1538
Certificate Number : R0-CEP 2001-354 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2004-10-11
Type : Chemical
Substance Number : 1538
Certificate Number : R1-CEP 2004-115 - Rev 03
Status : Valid
Issue Date : 2021-05-17
Type : Chemical
Substance Number : 1538
Certificate Number : R0-CEP 2006-161 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2011-11-08
Type : Chemical
Substance Number : 1538
Certificate Number : R1-CEP 2004-026 - Rev 03
Status : Valid
Issue Date : 2023-08-04
Type : Chemical
Substance Number : 1538
Certificate Number : R1-CEP 2004-191 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2010-12-02
Type : Chemical
Substance Number : 1538
Certificate Number : R1-CEP 2014-146 - Rev 00
Status : Valid
Issue Date : 2020-03-16
Type : Chemical
Substance Number : 1538
Certificate Number : R1-CEP 2001-406 - Rev 05
Status : Valid
Issue Date : 2021-07-02
Type : Chemical
Substance Number : 1538
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Certificate Number : CEP 2000-406 - Rev 06
Status : Valid
Issue Date : 2025-07-08
Type : Chemical
Substance Number : 1538
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
17
PharmaCompass offers a list of Lovastatin 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 Lovastatin manufacturer or Lovastatin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lovastatin manufacturer or Lovastatin supplier.
PharmaCompass also assists you with knowing the Lovastatin API Price utilized in the formulation of products. Lovastatin API Price is not always fixed or binding as the Lovastatin Price is obtained through a variety of data sources. The Lovastatin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lovastatine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lovastatine, including repackagers and relabelers. The FDA regulates Lovastatine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lovastatine 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 Lovastatine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lovastatine supplier is an individual or a company that provides Lovastatine active pharmaceutical ingredient (API) or Lovastatine finished formulations upon request. The Lovastatine suppliers may include Lovastatine API manufacturers, exporters, distributors and traders.
click here to find a list of Lovastatine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lovastatine CEP of the European Pharmacopoeia monograph is often referred to as a Lovastatine Certificate of Suitability (COS). The purpose of a Lovastatine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Lovastatine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Lovastatine to their clients by showing that a Lovastatine CEP has been issued for it. The manufacturer submits a Lovastatine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Lovastatine CEP holder for the record. Additionally, the data presented in the Lovastatine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Lovastatine DMF.
A Lovastatine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Lovastatine 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 Lovastatine suppliers with CEP (COS) on PharmaCompass.
We have 10 companies offering Lovastatine
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