01 1Hubei Meikai Chemical Co Ltd
02 1MakingCosmetics Inc.
03 1Vantage Specialty Chemicals, Inc.
04 1Yidu Huayang Chemical Co., Ltd. (Zhicheng Factory)
01 2OXYBENZONE
02 2Oxybenzone
01 2China
02 2U.S.A
NDC Package Code : 49464-0001
Start Marketing Date : 2016-06-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 61726-109
Start Marketing Date : 2017-12-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 80466-102
Start Marketing Date : 1997-11-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 13317-532
Start Marketing Date : 2011-11-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
16
PharmaCompass offers a list of Oxybenzone 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 Oxybenzone manufacturer or Oxybenzone supplier for your needs.
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A Escalol 567 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Escalol 567, including repackagers and relabelers. The FDA regulates Escalol 567 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Escalol 567 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Escalol 567 supplier is an individual or a company that provides Escalol 567 active pharmaceutical ingredient (API) or Escalol 567 finished formulations upon request. The Escalol 567 suppliers may include Escalol 567 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 Escalol 567 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Escalol 567 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 Escalol 567 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 Escalol 567 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Escalol 567 NDC to their finished compounded human drug products, they may choose to do so.
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We have 4 companies offering Escalol 567
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