Neuland Laboratories- A dedicated 100% API provider.
01 1Neuland Laboratories Limited
02 1Porton Pharma Solutions Ltd
03 1Curia Italy S.r.l.
04 1Harman Finochem Limited
01 1PROPOFOL
02 3Propofol
01 1China
02 2India
03 1U.S.A
Neuland Laboratories- A dedicated 100% API provider.
NDC Package Code : 58032-2019
Start Marketing Date : 2014-06-04
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Porton Pharma Solutions: Value creation via innovation & discovery through technical platforms.
NDC Package Code : 75877-0003
Start Marketing Date : 2013-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 44657-0044
Start Marketing Date : 2010-10-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66064-1015
Start Marketing Date : 2014-08-11
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
A Propofol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Propofol, including repackagers and relabelers. The FDA regulates Propofol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Propofol 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 Propofol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Propofol supplier is an individual or a company that provides Propofol active pharmaceutical ingredient (API) or Propofol finished formulations upon request. The Propofol suppliers may include Propofol API manufacturers, exporters, distributors and traders.
click here to find a list of Propofol 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 Propofol as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Propofol 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 Propofol 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 Propofol and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Propofol NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Propofol suppliers with NDC on PharmaCompass.
We have 4 companies offering Propofol
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