Home > National Drug Code (NDC) > Phenytoin Sodium

Phenytoin Sodium - 50268-660-15 - (Phenytoin Sodium)

Alphabetical Index


Drug Information of Phenytoin Sodium

Product NDC: 50268-660
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
Coding System: National Drug Codes(NDC)

Labeler Information of Phenytoin Sodium

Product NDC: 50268-660
Labeler Name: AvPAK
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040765
Marketing Category: ANDA
Start Marketing Date: 20091216

Package Information of Phenytoin Sodium

Package NDC: 50268-660-15
Package Description: 50 CAPSULE in 1 BOX, UNIT-DOSE (50268-660-15)

NDC Information of Phenytoin Sodium

NDC Code 50268-660-15
Proprietary Name Phenytoin Sodium
Package Description 50 CAPSULE in 1 BOX, UNIT-DOSE (50268-660-15)
Product NDC 50268-660
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phenytoin Sodium
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20091216
Marketing Category Name ANDA
Labeler Name AvPAK
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