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OXCARBAZEPINE - 51991-293-05 - (OXCARBAZEPINE)

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Drug Information of OXCARBAZEPINE

Product NDC: 51991-293
Proprietary Name: OXCARBAZEPINE
Non Proprietary Name: OXCARBAZEPINE
Active Ingredient(s): 300    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: 51991-293
Labeler Name: Breckenridge Pharmaceutical, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078069
Marketing Category: ANDA
Start Marketing Date: 20080111

Package Information of OXCARBAZEPINE

Package NDC: 51991-293-05
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (51991-293-05)

NDC Information of OXCARBAZEPINE

NDC Code 51991-293-05
Proprietary Name OXCARBAZEPINE
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (51991-293-05)
Product NDC 51991-293
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name OXCARBAZEPINE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080111
Marketing Category Name ANDA
Labeler Name Breckenridge Pharmaceutical, Inc.
Substance Name OXCARBAZEPINE
Strength Number 300
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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