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Phenytoin Sodium - 0409-1317-01 - (PHENYTOIN SODIUM)

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Drug Information of Phenytoin Sodium

Product NDC: 0409-1317
Proprietary Name: Phenytoin Sodium
Non Proprietary Name: PHENYTOIN SODIUM
Active Ingredient(s): 50    mg/mL & nbsp;   PHENYTOIN SODIUM
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Phenytoin Sodium

Product NDC: 0409-1317
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089521
Marketing Category: ANDA
Start Marketing Date: 20110217

Package Information of Phenytoin Sodium

Package NDC: 0409-1317-01
Package Description: 5 TRAY in 1 CONTAINER (0409-1317-01) > 5 AMPULE in 1 TRAY > 2 mL in 1 AMPULE

NDC Information of Phenytoin Sodium

NDC Code 0409-1317-01
Proprietary Name Phenytoin Sodium
Package Description 5 TRAY in 1 CONTAINER (0409-1317-01) > 5 AMPULE in 1 TRAY > 2 mL in 1 AMPULE
Product NDC 0409-1317
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PHENYTOIN SODIUM
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20110217
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
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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