Inke S.A: APIs manufacturing plant.
01 1Inke SA
02 1Veranova, L.P.
03 1Chongqing Biocare Pharmaceutical Ltd.
04 1MSN Laboratories Private Limited
01 1CLEVIDIPINE
02 1CLEVIDIPINE BUTYRATE
03 1Clevidipine
04 1Clevidipine Butyrate
01 1India
02 1Spain
03 1U.S.A
04 1Blank
NDC Package Code : 64567-0023
Start Marketing Date : 2021-01-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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 : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 33656-0013
Start Marketing Date : 2019-08-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Portfolio PDF
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Corporate PDF
A Clevidipine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clevidipine, including repackagers and relabelers. The FDA regulates Clevidipine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clevidipine 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 Clevidipine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Clevidipine supplier is an individual or a company that provides Clevidipine active pharmaceutical ingredient (API) or Clevidipine finished formulations upon request. The Clevidipine suppliers may include Clevidipine API manufacturers, exporters, distributors and traders.
click here to find a list of Clevidipine 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 Clevidipine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Clevidipine 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 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 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Clevidipine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Clevidipine suppliers with NDC on PharmaCompass.
We have 3 companies offering Clevidipine
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