01 1B.V. KATWIJK CHEMIE
02 1Harman Finochem Limited
03 1Medisca Inc.
04 1Pharmacia and Upjohn Company LLC
05 1Professional Compounding Centers of America
06 1RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA
07 1Spectrum Laboratory Products, Inc.
08 1Swati Spentose Private Limited
09 1Unichem Laboratories Limited, India
01 2PHENYTOIN SODIUM
02 7Phenytoin Sodium
01 3India
02 1Italy
03 1Netherlands
04 3U.S.A
05 1United Kingdom
NDC Package Code : 66064-6001
Start Marketing Date : 2004-11-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17349-0004
Start Marketing Date : 1984-06-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0216
Start Marketing Date : 2014-06-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0301
Start Marketing Date : 2023-04-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 0009-0087
Start Marketing Date : 2013-12-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12711-4466
Start Marketing Date : 1969-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 49452-5344
Start Marketing Date : 1995-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52119-006
Start Marketing Date : 2012-08-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53747-082
Start Marketing Date : 2018-03-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Dilantin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dilantin, including repackagers and relabelers. The FDA regulates Dilantin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dilantin 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 Dilantin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dilantin supplier is an individual or a company that provides Dilantin active pharmaceutical ingredient (API) or Dilantin finished formulations upon request. The Dilantin suppliers may include Dilantin API manufacturers, exporters, distributors and traders.
click here to find a list of Dilantin 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 Dilantin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Dilantin 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 Dilantin 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 Dilantin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Dilantin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Dilantin suppliers with NDC on PharmaCompass.
We have 9 companies offering Dilantin
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