Home > National Drug Code (NDC) > fosphenytoin sodium

fosphenytoin sodium - 0517-6902-10 - (fosphenytoin sodium)

Alphabetical Index


Drug Information of fosphenytoin sodium

Product NDC: 0517-6902
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: 0517-6902
Labeler Name: American Regent, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090099
Marketing Category: ANDA
Start Marketing Date: 20100730

Package Information of fosphenytoin sodium

Package NDC: 0517-6902-10
Package Description: 10 VIAL in 1 BOX (0517-6902-10) > 2 mL in 1 VIAL

NDC Information of fosphenytoin sodium

NDC Code 0517-6902-10
Proprietary Name fosphenytoin sodium
Package Description 10 VIAL in 1 BOX (0517-6902-10) > 2 mL in 1 VIAL
Product NDC 0517-6902
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fosphenytoin sodium
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20100730
Marketing Category Name ANDA
Labeler Name American Regent, 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


General Information