01 1Chongqing Daxin Pharmaceutical Co., Ltd.
02 1Concord Biotech Limited
03 1DARMERICA, LLC
04 1LIVZON NEW NORTH RIVER PHARMACEUTICAL CO.,LTD.
05 2TAPI Hungary Industries Kft.
06 2Teva Pharmaceutical Works Private Limited Company
07 1Zhejiang Hisun Pharmaceutical Co., Ltd.
01 9Lovastatin
01 2China
02 1India
03 2Israel
04 1U.S.A
05 3Blank
NDC Package Code : 68254-0001
Start Marketing Date : 2006-04-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71052-668
Start Marketing Date : 2020-09-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100g/100g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 20076-0402
Start Marketing Date : 2015-05-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51846-1014
Start Marketing Date : 2019-08-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51846-1040
Start Marketing Date : 2013-01-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 58623-0021
Start Marketing Date : 1996-09-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 84671-1040
Start Marketing Date : 2013-01-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
NDC Package Code : 57885-0008
Start Marketing Date : 2019-10-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
NDC Package Code : 84671-1014
Start Marketing Date : 2019-08-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
A Lovastatin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lovastatin, including repackagers and relabelers. The FDA regulates Lovastatin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lovastatin 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 Lovastatin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lovastatin supplier is an individual or a company that provides Lovastatin active pharmaceutical ingredient (API) or Lovastatin finished formulations upon request. The Lovastatin suppliers may include Lovastatin API manufacturers, exporters, distributors and traders.
click here to find a list of Lovastatin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Lovastatin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Lovastatin API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Lovastatin as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Lovastatin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Lovastatin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Lovastatin suppliers with NDC on PharmaCompass.
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