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Oxcarbazepine - 62756-185-18 - (Oxcarbazepine)

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Drug Information of Oxcarbazepine

Product NDC: 62756-185
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: 62756-185
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077794
Marketing Category: ANDA
Start Marketing Date: 20071009

Package Information of Oxcarbazepine

Package NDC: 62756-185-18
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (62756-185-18)

NDC Information of Oxcarbazepine

NDC Code 62756-185-18
Proprietary Name Oxcarbazepine
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (62756-185-18)
Product NDC 62756-185
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 Sun Pharmaceutical Industries Limited
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


General Information