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Oxcarbazepine - 54868-6129-0 - (Oxcarbazepine)

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Drug Information of Oxcarbazepine

Product NDC: 54868-6129
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: 54868-6129
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077802
Marketing Category: ANDA
Start Marketing Date: 20100623

Package Information of Oxcarbazepine

Package NDC: 54868-6129-0
Package Description: 10 TABLET, FILM COATED in 1 BOTTLE (54868-6129-0)

NDC Information of Oxcarbazepine

NDC Code 54868-6129-0
Proprietary Name Oxcarbazepine
Package Description 10 TABLET, FILM COATED in 1 BOTTLE (54868-6129-0)
Product NDC 54868-6129
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxcarbazepine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100623
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
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


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