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 : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48041-0002
Start Marketing Date : 2014-09-22
End Marketing Date : 2025-12-31
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
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PharmaCompass offers a list of Levomenthol 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 Levomenthol manufacturer or Levomenthol supplier for your needs.
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A Tox21_202608 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_202608, including repackagers and relabelers. The FDA regulates Tox21_202608 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_202608 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_202608 supplier is an individual or a company that provides Tox21_202608 active pharmaceutical ingredient (API) or Tox21_202608 finished formulations upon request. The Tox21_202608 suppliers may include Tox21_202608 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 Tox21_202608 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Tox21_202608 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_202608 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_202608 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tox21_202608 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Tox21_202608 suppliers with NDC on PharmaCompass.
We have 4 companies offering Tox21_202608
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