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Oxcarbazepine - 0781-6270-43 - (oxcarbazepine)

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Drug Information of Oxcarbazepine

Product NDC: 0781-6270
Proprietary Name: Oxcarbazepine
Non Proprietary Name: oxcarbazepine
Active Ingredient(s): 60    mg/mL & nbsp;   oxcarbazepine
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Oxcarbazepine

Product NDC: 0781-6270
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021285
Marketing Category: NDA
Start Marketing Date: 20010530

Package Information of Oxcarbazepine

Package NDC: 0781-6270-43
Package Description: 250 mL in 1 BOTTLE (0781-6270-43)

NDC Information of Oxcarbazepine

NDC Code 0781-6270-43
Proprietary Name Oxcarbazepine
Package Description 250 mL in 1 BOTTLE (0781-6270-43)
Product NDC 0781-6270
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxcarbazepine
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20010530
Marketing Category Name NDA
Labeler Name Sandoz Inc
Substance Name OXCARBAZEPINE
Strength Number 60
Strength Unit mg/mL
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Oxcarbazepine


General Information