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01 1Fermion Oy
02 1Jagsonpal Pharmaceuticals Limited
03 1Professional Compounding Centers of America dba PCCA
04 1Spectrum Laboratory Products, Inc.
05 1Zen Chemicals Private Limited
01 1TOLNAFTATE
02 3Tolnaftate
03 1tolnaftate
01 1Finland
02 1India
03 1Japan
04 1U.S.A
05 1United Kingdom
NDC Package Code : 12780-4800
Start Marketing Date : 1985-04-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53934-0009
Start Marketing Date : 2012-05-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0039
Start Marketing Date : 2019-12-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-7834
Start Marketing Date : 1993-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 72742-3500
Start Marketing Date : 2019-10-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Tolnaftate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tolnaftate, including repackagers and relabelers. The FDA regulates Tolnaftate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tolnaftate 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 Tolnaftate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tolnaftate supplier is an individual or a company that provides Tolnaftate active pharmaceutical ingredient (API) or Tolnaftate finished formulations upon request. The Tolnaftate suppliers may include Tolnaftate API manufacturers, exporters, distributors and traders.
click here to find a list of Tolnaftate 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 Tolnaftate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Tolnaftate 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 Tolnaftate 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 Tolnaftate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tolnaftate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Tolnaftate suppliers with NDC on PharmaCompass.
We have 5 companies offering Tolnaftate
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