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OXCARBAZEPINE - 63629-3816-2 - (OXCARBAZEPINE)

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Drug Information of OXCARBAZEPINE

Product NDC: 63629-3816
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: 63629-3816
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078069
Marketing Category: ANDA
Start Marketing Date: 20080111

Package Information of OXCARBAZEPINE

Package NDC: 63629-3816-2
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (63629-3816-2)

NDC Information of OXCARBAZEPINE

NDC Code 63629-3816-2
Proprietary Name OXCARBAZEPINE
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (63629-3816-2)
Product NDC 63629-3816
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 Bryant Ranch Prepack
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


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