Oxcarbazepine

Product NDC

0615-6593

11-digit product format

006156593

Labeler code

0615

Product ID

0615-6593_ec0eb04b-6d9d-4336-952b-376b19535d8e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxcarbazepine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA077794

Marketing category

ANDA

Marketing start

2007-10-09

Marketing end

0000-00-00

Substance

OXCARBAZEPINE

Active strength

150 mg/1

Pharmacologic classes

Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record