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Phenytoin Sodium - 55154-7461-5 - (Phenytoin Sodium)

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Drug Information of Phenytoin Sodium

Product NDC: 55154-7461
Proprietary Name: Phenytoin Sodium
Non Proprietary Name: Phenytoin Sodium
Active Ingredient(s): 50    mg/mL & nbsp;   Phenytoin Sodium
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Phenytoin Sodium

Product NDC: 55154-7461
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040573
Marketing Category: ANDA
Start Marketing Date: 20061001

Package Information of Phenytoin Sodium

Package NDC: 55154-7461-5
Package Description: 5 VIAL in 1 BAG (55154-7461-5) > 2 mL in 1 VIAL

NDC Information of Phenytoin Sodium

NDC Code 55154-7461-5
Proprietary Name Phenytoin Sodium
Package Description 5 VIAL in 1 BAG (55154-7461-5) > 2 mL in 1 VIAL
Product NDC 55154-7461
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phenytoin Sodium
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20061001
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name PHENYTOIN SODIUM
Strength Number 50
Strength Unit mg/mL
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Phenytoin Sodium


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