01 1Alivira Animal Health Limited
02 1Hubei Honch Pharmaceutical Co., Ltd.
03 1LAURUS SYNTHESIS PVT LTD
04 1Lonza AG
01 2LUFENURON
02 2Lufenuron
01 1China
02 2India
03 1U.S.A
NDC Package Code : 86055-0029
Start Marketing Date : 2023-05-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62158-0004
Start Marketing Date : 2018-11-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69843-001
Start Marketing Date : 2024-04-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49187-0300
Start Marketing Date : 2011-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Lufenuron 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 Lufenuron manufacturer or Lufenuron supplier for your needs.
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PharmaCompass also assists you with knowing the Lufenuron API Price utilized in the formulation of products. Lufenuron API Price is not always fixed or binding as the Lufenuron Price is obtained through a variety of data sources. The Lufenuron Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tox21_300907 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300907, including repackagers and relabelers. The FDA regulates Tox21_300907 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300907 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 Tox21_300907 supplier is an individual or a company that provides Tox21_300907 active pharmaceutical ingredient (API) or Tox21_300907 finished formulations upon request. The Tox21_300907 suppliers may include Tox21_300907 API manufacturers, exporters, distributors and traders.
click here to find a list of Tox21_300907 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 Tox21_300907 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Tox21_300907 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 Tox21_300907 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 Tox21_300907 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tox21_300907 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Tox21_300907 suppliers with NDC on PharmaCompass.
We have 4 companies offering Tox21_300907
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