Home > National Drug Code (NDC) > Phenytoin Sodium

Phenytoin Sodium - 63629-2552-2 - (phenytoin sodium)

Alphabetical Index


Drug Information of Phenytoin Sodium

Product NDC: 63629-2552
Proprietary Name: Phenytoin Sodium
Non Proprietary Name: phenytoin sodium
Active Ingredient(s): 100    mg/1 & nbsp;   phenytoin sodium
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Phenytoin Sodium

Product NDC: 63629-2552
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040298
Marketing Category: ANDA
Start Marketing Date: 20110707

Package Information of Phenytoin Sodium

Package NDC: 63629-2552-2
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-2552-2)

NDC Information of Phenytoin Sodium

NDC Code 63629-2552-2
Proprietary Name Phenytoin Sodium
Package Description 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-2552-2)
Product NDC 63629-2552
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name phenytoin sodium
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110707
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name PHENYTOIN SODIUM
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Phenytoin Sodium


General Information