Veranova: A CDMO that manages complexity with confidence.
01 1Veranova, L.P.
02 1Chongqing Biocare Pharmaceutical Ltd.
03 1MSN Laboratories Private Limited
04 1Zhongfu Pharmaceutical Co., Ltd.
01 2CLEVIDIPINE
02 1Clevidipine
03 1Clevidipine Butyrate
01 1India
02 1U.S.A
03 2Blank
Veranova: A CDMO that manages complexity with confidence.
NDC Package Code : 50137-2930
Start Marketing Date : 2008-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14501-0080
Start Marketing Date : 2014-04-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 33656-0013
Start Marketing Date : 2019-08-01
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 : 63673-0001
Start Marketing Date : 2018-03-16
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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PharmaCompass offers a list of Clevidipine 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 Clevidipine manufacturer or Clevidipine supplier for your needs.
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A Clevidipine Butyrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clevidipine Butyrate, including repackagers and relabelers. The FDA regulates Clevidipine Butyrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clevidipine Butyrate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Clevidipine Butyrate supplier is an individual or a company that provides Clevidipine Butyrate active pharmaceutical ingredient (API) or Clevidipine Butyrate finished formulations upon request. The Clevidipine Butyrate suppliers may include Clevidipine Butyrate API manufacturers, exporters, distributors and traders.
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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 Clevidipine Butyrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Clevidipine Butyrate 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 Clevidipine Butyrate 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 Clevidipine Butyrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Clevidipine Butyrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Clevidipine Butyrate suppliers with NDC on PharmaCompass.
We have 2 companies offering Clevidipine Butyrate
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