Home > National Drug Code (NDC) > Fosphenytoin Sodium

Fosphenytoin Sodium - 55390-176-10 - (Fosphenytoin Sodium)

Alphabetical Index


Drug Information of Fosphenytoin Sodium

Product NDC: 55390-176
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: 55390-176
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077481
Marketing Category: ANDA
Start Marketing Date: 20070806

Package Information of Fosphenytoin Sodium

Package NDC: 55390-176-10
Package Description: 10 VIAL in 1 BOX (55390-176-10) > 10 mL in 1 VIAL

NDC Information of Fosphenytoin Sodium

NDC Code 55390-176-10
Proprietary Name Fosphenytoin Sodium
Package Description 10 VIAL in 1 BOX (55390-176-10) > 10 mL in 1 VIAL
Product NDC 55390-176
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fosphenytoin Sodium
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20070806
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
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


General Information