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OXTELLAR XR - 17772-123-01 - (OXCARBAZEPINE)

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Drug Information of OXTELLAR XR

Product NDC: 17772-123
Proprietary Name: OXTELLAR XR
Non Proprietary Name: OXCARBAZEPINE
Active Ingredient(s): 600    mg/1 & nbsp;   OXCARBAZEPINE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of OXTELLAR XR

Product NDC: 17772-123
Labeler Name: Supernus
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA202810
Marketing Category: NDA
Start Marketing Date: 20130117

Package Information of OXTELLAR XR

Package NDC: 17772-123-01
Package Description: 100 TABLET in 1 BOTTLE (17772-123-01)

NDC Information of OXTELLAR XR

NDC Code 17772-123-01
Proprietary Name OXTELLAR XR
Package Description 100 TABLET in 1 BOTTLE (17772-123-01)
Product NDC 17772-123
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name OXCARBAZEPINE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130117
Marketing Category Name NDA
Labeler Name Supernus
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 OXTELLAR XR


General Information