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Fosphenytoin Sodium - 47335-834-01 - (Fosphenytoin Sodium)

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Drug Information of Fosphenytoin Sodium

Product NDC: 47335-834
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: 47335-834
Labeler Name: Sun Pharma Global FZE
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078417
Marketing Category: ANDA
Start Marketing Date: 20090814

Package Information of Fosphenytoin Sodium

Package NDC: 47335-834-01
Package Description: 10 VIAL, SINGLE-DOSE in 1 CARTON (47335-834-01) > 10 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Fosphenytoin Sodium

NDC Code 47335-834-01
Proprietary Name Fosphenytoin Sodium
Package Description 10 VIAL, SINGLE-DOSE in 1 CARTON (47335-834-01) > 10 mL in 1 VIAL, SINGLE-DOSE
Product NDC 47335-834
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fosphenytoin Sodium
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20090814
Marketing Category Name ANDA
Labeler Name Sun Pharma Global FZE
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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