01 1DARMERICA, LLC
02 1Qingdao Biopeptek Co., Ltd.
03 1Qingdao Qinzeyuan Biotechnology Co., Ltd
01 3Amlexanox
01 1U.S.A
02 2Blank
NDC Package Code : 73212-078
Start Marketing Date : 2023-10-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71052-005
Start Marketing Date : 2019-08-13
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (100g/100g)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
NDC Package Code : 85512-2006
Start Marketing Date : 2025-05-12
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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PharmaCompass offers a list of Amlexanox 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 Amlexanox manufacturer or Amlexanox supplier for your needs.
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PharmaCompass also assists you with knowing the Amlexanox API Price utilized in the formulation of products. Amlexanox API Price is not always fixed or binding as the Amlexanox Price is obtained through a variety of data sources. The Amlexanox Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MLS006010129 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MLS006010129, including repackagers and relabelers. The FDA regulates MLS006010129 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MLS006010129 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 MLS006010129 supplier is an individual or a company that provides MLS006010129 active pharmaceutical ingredient (API) or MLS006010129 finished formulations upon request. The MLS006010129 suppliers may include MLS006010129 API manufacturers, exporters, distributors and traders.
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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 MLS006010129 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for MLS006010129 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 MLS006010129 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 MLS006010129 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a MLS006010129 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of MLS006010129 suppliers with NDC on PharmaCompass.
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