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Fosphenytoin Sodium - 0409-4857-10 - (FOSPHENYTOIN SODIUM)

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Drug Information of Fosphenytoin Sodium

Product NDC: 0409-4857
Proprietary Name: Fosphenytoin Sodium
Non Proprietary Name: FOSPHENYTOIN SODIUM
Active Ingredient(s): 50    mg/mL & nbsp;   FOSPHENYTOIN SODIUM
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Fosphenytoin Sodium

Product NDC: 0409-4857
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078158
Marketing Category: ANDA
Start Marketing Date: 20110708

Package Information of Fosphenytoin Sodium

Package NDC: 0409-4857-10
Package Description: 10 VIAL, GLASS in 1 CARTON (0409-4857-10) > 10 mL in 1 VIAL, GLASS

NDC Information of Fosphenytoin Sodium

NDC Code 0409-4857-10
Proprietary Name Fosphenytoin Sodium
Package Description 10 VIAL, GLASS in 1 CARTON (0409-4857-10) > 10 mL in 1 VIAL, GLASS
Product NDC 0409-4857
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name FOSPHENYTOIN SODIUM
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20110708
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name FOSPHENYTOIN 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 Fosphenytoin Sodium


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