01 1Anhui Yinfeng Pharmaceutical Co., Ltd.
02 2BASF SE
03 1Josun International Limited
04 1Spectrum Laboratory Products, Inc.
01 1L-Menthol
02 1L-Menthol Pharma
03 1L-Menthol Pharma Flakes
04 2Menthol
01 2China
02 2Germany
03 1U.S.A
NDC Package Code : 69155-003
Start Marketing Date : 2023-05-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48041-0001
Start Marketing Date : 2014-07-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48041-0002
Start Marketing Date : 2014-09-22
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51551-0308
Start Marketing Date : 2023-05-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-4440
Start Marketing Date : 1990-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Hexahydrothymol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hexahydrothymol, including repackagers and relabelers. The FDA regulates Hexahydrothymol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hexahydrothymol 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 Hexahydrothymol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hexahydrothymol supplier is an individual or a company that provides Hexahydrothymol active pharmaceutical ingredient (API) or Hexahydrothymol finished formulations upon request. The Hexahydrothymol suppliers may include Hexahydrothymol API manufacturers, exporters, distributors and traders.
click here to find a list of Hexahydrothymol 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 Hexahydrothymol as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Hexahydrothymol 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 Hexahydrothymol 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 Hexahydrothymol and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Hexahydrothymol NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Hexahydrothymol suppliers with NDC on PharmaCompass.
We have 4 companies offering Hexahydrothymol
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