01 1ARXADA, LLC
02 1DISHMAN CARBOGEN AMCIS LIMITED
03 1Lonza, LLC
04 1Organo Sintesis, S.A. de C.V.
05 1Pilot Chemical Company
01 1BENZETHONIUM CHLORIDE
02 4Benzethonium Chloride
01 1India
02 1Mexico
03 2Switzerland
04 1U.S.A
NDC Package Code : 69284-008
Start Marketing Date : 2022-12-06
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 61876-0016
Start Marketing Date : 2011-06-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69284-002
Start Marketing Date : 2016-02-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51606-003
Start Marketing Date : 2023-12-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 73602-010
Start Marketing Date : 2024-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Benzethonium Chloride 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 Benzethonium Chloride manufacturer or Benzethonium Chloride supplier for your needs.
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PharmaCompass also assists you with knowing the Benzethonium Chloride API Price utilized in the formulation of products. Benzethonium Chloride API Price is not always fixed or binding as the Benzethonium Chloride Price is obtained through a variety of data sources. The Benzethonium Chloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Diisobutyl phenoxy ethoxy ethyl dimethyl benzyl ammonium chloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diisobutyl phenoxy ethoxy ethyl dimethyl benzyl ammonium chloride, including repackagers and relabelers. The FDA regulates Diisobutyl phenoxy ethoxy ethyl dimethyl benzyl ammonium chloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diisobutyl phenoxy ethoxy ethyl dimethyl benzyl ammonium chloride 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 Diisobutyl phenoxy ethoxy ethyl dimethyl benzyl ammonium chloride supplier is an individual or a company that provides Diisobutyl phenoxy ethoxy ethyl dimethyl benzyl ammonium chloride active pharmaceutical ingredient (API) or Diisobutyl phenoxy ethoxy ethyl dimethyl benzyl ammonium chloride finished formulations upon request. The Diisobutyl phenoxy ethoxy ethyl dimethyl benzyl ammonium chloride suppliers may include Diisobutyl phenoxy ethoxy ethyl dimethyl benzyl ammonium chloride API manufacturers, exporters, distributors and traders.
click here to find a list of Diisobutyl phenoxy ethoxy ethyl dimethyl benzyl ammonium chloride 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 Diisobutyl phenoxy ethoxy ethyl dimethyl benzyl ammonium chloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Diisobutyl phenoxy ethoxy ethyl dimethyl benzyl ammonium chloride 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 Diisobutyl phenoxy ethoxy ethyl dimethyl benzyl ammonium chloride 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 Diisobutyl phenoxy ethoxy ethyl dimethyl benzyl ammonium chloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Diisobutyl phenoxy ethoxy ethyl dimethyl benzyl ammonium chloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Diisobutyl phenoxy ethoxy ethyl dimethyl benzyl ammonium chloride suppliers with NDC on PharmaCompass.
We have 5 companies offering Diisobutyl phenoxy ethoxy ethyl dimethyl benzyl ammonium chloride
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