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Oxcarbazepine - 21695-862-30 - (Oxcarbazepine)

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Drug Information of Oxcarbazepine

Product NDC: 21695-862
Proprietary Name: Oxcarbazepine
Non Proprietary Name: Oxcarbazepine
Active Ingredient(s): 150    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: 21695-862
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077802
Marketing Category: ANDA
Start Marketing Date: 20071009

Package Information of Oxcarbazepine

Package NDC: 21695-862-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (21695-862-30)

NDC Information of Oxcarbazepine

NDC Code 21695-862-30
Proprietary Name Oxcarbazepine
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (21695-862-30)
Product NDC 21695-862
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxcarbazepine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20071009
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name OXCARBAZEPINE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Oxcarbazepine


General Information