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Oxcarbazepine - 60505-2536-1 - (Oxcarbazepine)

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Drug Information of Oxcarbazepine

Product NDC: 60505-2536
Proprietary Name: Oxcarbazepine
Non Proprietary Name: Oxcarbazepine
Active Ingredient(s): 600    mg/1 & nbsp;   Oxcarbazepine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Oxcarbazepine

Product NDC: 60505-2536
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077747
Marketing Category: ANDA
Start Marketing Date: 20080409

Package Information of Oxcarbazepine

Package NDC: 60505-2536-1
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (60505-2536-1)

NDC Information of Oxcarbazepine

NDC Code 60505-2536-1
Proprietary Name Oxcarbazepine
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (60505-2536-1)
Product NDC 60505-2536
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxcarbazepine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080409
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name OXCARBAZEPINE
Strength Number 600
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Oxcarbazepine


General Information