Oxcarbazepine

Product NDC

50090-3961

11-digit product format

500903961

Labeler code

50090

Product ID

50090-3961_81ab1371-4617-4376-8776-1c9ee1bd854b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxcarbazepine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA077802

Marketing category

ANDA

Marketing start

2007-10-09

Marketing end

0000-00-00

Substance

OXCARBAZEPINE

Active strength

300 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record