Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
01 1Bachem SA, succursale de Vionnaz
02 1Huzhou Zhanwang Pharmaceutical Co., Ltd.
01 1ETOMIDATE
02 1Etomidate
01 1China
02 1Switzerland
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
NDC Package Code : 51504-0012
Start Marketing Date : 2007-01-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63660-0005
Start Marketing Date : 2011-03-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Etomidate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Etomidate, including repackagers and relabelers. The FDA regulates Etomidate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Etomidate 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 Etomidate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Etomidate supplier is an individual or a company that provides Etomidate active pharmaceutical ingredient (API) or Etomidate finished formulations upon request. The Etomidate suppliers may include Etomidate API manufacturers, exporters, distributors and traders.
click here to find a list of Etomidate 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 Etomidate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Etomidate 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 Etomidate 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 Etomidate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Etomidate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Etomidate suppliers with NDC on PharmaCompass.
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