Veranova: A CDMO that manages complexity with confidence.
01 1Veranova, L.P.
02 1Fine Chemicals Corporation (PTY) Ltd.
03 1American Pacific Corporation
04 1Cilag AG
05 1Navinta LLC, NJ, USA
01 2Remifentanil HCl
02 2Remifentanil Hydrochloride
03 1Remifentanil hydrochloride
01 1South Africa
02 1Switzerland
03 3U.S.A
NDC Package Code : 49812-0190
Start Marketing Date : 2012-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48954-724
Start Marketing Date : 2007-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50683-0550
Start Marketing Date : 2020-10-22
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12502-5343
Start Marketing Date : 2013-12-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 68475-021
Start Marketing Date : 2020-07-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (500g/500g)
Marketing Category : BULK INGREDIENT
A Remifentanil Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Remifentanil Hydrochloride, including repackagers and relabelers. The FDA regulates Remifentanil Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Remifentanil Hydrochloride 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 Remifentanil Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Remifentanil Hydrochloride supplier is an individual or a company that provides Remifentanil Hydrochloride active pharmaceutical ingredient (API) or Remifentanil Hydrochloride finished formulations upon request. The Remifentanil Hydrochloride suppliers may include Remifentanil Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Remifentanil Hydrochloride 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 Remifentanil Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Remifentanil Hydrochloride 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 Remifentanil Hydrochloride 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 Remifentanil Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Remifentanil Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Remifentanil Hydrochloride suppliers with NDC on PharmaCompass.
We have 5 companies offering Remifentanil Hydrochloride
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